Castor Catalyst is the first to market to show industry-leading data extraction accuracy in a sponsor-audit-friendly technical approach

September 3rd, 2026 by

Castor Catalyst is Castor’s AI-driven clinical data platform that reads data straight from source records and proposes each value for a human to review. Across studies in five countries, reviewers accepted more than 99 percent of what Catalyst extracted, evidence that AI can meet the data standards of regulated research while a person stays in control of the record.

NEW YORK, September 3, 2026 Castor today announced a milestone for Castor Catalyst, its AI-driven clinical data platform that extracts data directly from source records under human review. In a recent study for a live commercial production study, human reviewers accepted ~99% of the values Catalyst extracted, overriding 0.78 percent.

Catalyst is live in production across five countries, in studies spanning real-world evidence, post-market clinical follow-up (PMCF), and pivotal medical device trials. Instead of teams re-keying source documents into their EDC by hand, Catalyst reads the source, extracts the data, and presents it in a reviewer-friendly interface that keeps the original context. The reviewer keeps, corrects, or rejects each value before it enters the clinical record.

Extracting data directly from source records with AI is not widely used in regulated research, where every value has to withstand audit. Catalyst uses a Google Gemini model with data residency in the United States and the European Union. Personal data is redacted through Catalyst’s proprietary localized pseudonymization before anything is processed. Castor operates under zero data retention, and no client data is used to train models. Catalyst is GxP compliant, designed to meet ICH E6(R3) GCP, 21 CFR Part 11, and EU Annex 11, with a full immutable audit trail and mandatory human review.

In that commercial production study, reviewers assessed 14,290 data points Catalyst extracted from 285 source files across 158 participants. They accepted 99.16 percent as extracted and overrode 0.78 percent, submitting 14,282 values to the clinical database with no upload errors. Each value was shown to a reviewer against its source before submission, so the low override rate reflects review, not unchecked pass-through. In internal EMR benchmarking of site-based chart review, Catalyst reduced the work from 39 minutes to 6 minutes per chart.

“The need for automation in clinical trials is greater than ever, with budget pressure and staff burnout more common than ever. Yet using AI in clinical trials, especially in day-to-day clinical operations, is not an easy task. With Catalyst, I believe we have found the right blend of compliant, auditable AI combined with human oversight. Seeing AI actually make an impact on real clinical operations is something we are really proud of.”Derk Arts, Founder and CEO, Castor

“Using AI to enter data directly from source records is not widely utilized for regulated research outside of recruitment, because it has to clear a high bar. When reviewers accept more than 99 percent of what the AI extracts, across studies in five countries, it shows the approach works and holds up to the standards that clinical trials, real-world evidence, and med tech all demand. The demand we are seeing tells us research teams have been waiting for this, real speed with a human in charge.”Lisa Charlton, Chief Product Officer, Castor

About Castor

Castor is a clinical trial data platform for medical device, biopharma, diagnostics, and academic research teams. From site-based studies to fully decentralized, direct-to-patient designs, Castor unifies EDC, eCOA and ePRO, eConsent, data management, and Catalyst AI in one compliant platform. Learn more at castoredc.com, or explore Catalyst.

Media contact
Kevin Thornton, Director of Marketing, Castor
[email protected]

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Derk Arts wants to make data entry for medical research affordable

November 2nd, 2015 by

Editor’s note: this interview was first published in November 2015, by Rob Konterman. We are republishing it in 2026, with the original conversation kept largely intact and a short update at the end on what came next. The original is also archived on Fast Moving Targets.

The original interview

Derk Arts built the first version of Castor EDC himself. The online application, where users can easily set up a database to collect medical data, saw to his needs at the time. During his study to become a Medical Doctor (MD) he was obliged to conduct research. The data, collected by several people, was recorded in Excel sheets. “One Excel sheet per person. With my IT background I was convinced that there was an easier way. But when I asked around I soon learned that this was the usual way to process data. At this point I thought: this is not right. That’s how I gradually got involved in the field.”

The affordable solution that can be used by anyone

It turned out that the necessary products were available but they were really aimed at the pharmaceutical industry, not the medical world. “First of all they were extremely expensive. The average physician who wanted to conduct research could not afford it. Plus it involves a lengthy and complicated process with quotations and contracts that often results in complex systems requiring programming knowledge to use correctly. So we decided to build a system that is both affordable and easy to use, so everyone can use it.” And so it happened. Castor was quickly adopted by a growing community of researchers across hundreds of studies.

“To make a really good product that is of meaning to the community.”

Castor was growing fast in the Netherlands. “Many people see the advantage of an affordable solution that can be used by anyone. The difference between our system and the use of Excel for data collection is enormous. The quality of the data really increases tremendously and offers more potential for re-use, which means less research waste, as we call it. So yes, things are moving very fast. We are talking with numerous people and research institutes and we already have users in hospitals across the Netherlands.” And the international market was beckoning. “But first we will have to do extensive research to find out what is and isn’t allowed in other countries. It is challenging and interesting but also very difficult. It is much easier to have a consumer product that everyone can use without any regulations.”

What drove the work was the mission, not the margin. “I want to make a really good product that contributes to the community. I want to make Castor more and more affordable so everyone in the world can use it. In the Netherlands there is quite a bit of money available for research but in Brazil this might be different. I want them to be able to use it as well.”

“The difference between Castor and Excel is enormous. Data quality increases and there is less research waste.”

Storing data was just one part of the picture. For the graphical display and analysis that came afterwards, Castor at the time preferred to have the latter done by other parties, and there was already very good open source analysis software available. On visualization, Arts saw opportunities. “Recently I came across a very interesting American start-up whose core business was visualization. The only thing they do is the visualization of ongoing trials. So maybe we might say: this is our API, let’s connect, let’s be modern. But they will have to fit into our ideology, as normally these parties are extremely expensive. If this is the case we will do this part ourselves as well, even though it is not always simple.” Even then, data could be collected with the help of personal equipment, such as a Fitbit. “This information is very valuable but without standardization it is a lot of work to correctly use this data. We definitely want to play an important role and structure all such incoming data so it can be used for research. Research requires structured data. I believe that it would also be a good thing to think about standardization before bombarding the world with all kinds of platforms and devices and portals.”

“Doing something in which you believe and that ignites your passion makes a big difference.”

The biggest challenge, however, was to extend what had been achieved in the Netherlands across borders. “Science is science across the globe and normally this always goes by the same rules.” Arts had a positive look on the future. He no longer programs anything himself, and he does nothing with his medical training, but he is working on something he believes in, for the full 100%. “I have learned from other successful companies that having the ideology and doing something you believe in and what ignites your passion makes a big difference. I think this is really important, plus I like to try and play my part in society. What I mean is: I am an MD. It took me 7 years and now I do nothing with it, resulting in many questions from people around me. When are you going to specialize? But that is not going to happen. So I am hoping to make a difference to healthcare in a different way. And also for the patients, of course. You have to make decisions in life.”

The job was always better decisions. The tool became AI.

More than a decade on, the mission Derk described has not changed: make clinical research data good enough to trust, and usable by any research team, not just big pharma. What has changed is what the software can carry.

Making data entry affordable was step one. The bigger prize was always getting the manual work off people entirely. That is what Castor Catalyst does now: AI-driven clinical data extraction, with human reviewers in the loop by design and in control of what enters the record. Same goal as 2015, better data for more teams, with the manual work handed to the machine and people keeping oversight.

The through-line runs from Derk’s PhD at the University of Amsterdam, on improving medical decision making, through a platform any researcher could use to capture data well, to AI doing the parts that were never a good use of a person’s time.

“The point was never to hand clinical data to a machine and step back. It’s the opposite. Let AI do the manual work that was never a good use of a researcher’s time, and keep people in control of what the data actually says. Made with AI, not by AI. It’s the same thing I’ve chased since my PhD: better data, better decisions, with people spending their time on the judgment, not the data entry.”

Castor has grown far beyond that early Netherlands team. The platform now runs clinical data management end to end, with Catalyst at the center of the offer. Its work today spans medical device and PMCF research, biotech and biopharma trials, diagnostics, and academic research teams. The belief underneath has not changed. Better data leads to better decisions.

For more on Castor and where it is headed, see About Castor.

FAQ

Who is Derk Arts?
Derk Arts is the founder of Castor and a physician-researcher (MD PhD). He earned his PhD at the University of Amsterdam on improving medical decision making, and founded Castor in 2012 to make clinical research data easier to capture and trust.

When was Castor founded?
Castor was founded in 2012 by Derk Arts. It is a clinical trial data platform for medical device, biopharma, diagnostics, and academic research teams.

What is Castor Catalyst?
Castor Catalyst is Castor’s AI-driven clinical data extraction capability. The AI reads and structures clinical data, with human reviewers in the loop by design and in control of what enters the record.

Castor Inks Big Pharma Deal As Decentralized Trials Business Continues to Show Exponential Growth

March 10th, 2021 by

Hoboken, New Jersey: March 10, 2021: Castor, a leading provider of clinical trial technology, today announced the signing of a top-5 pharmaceutical company and expansion of its global team. 

2020 was a defining year for Castor. The company launched its scalable decentralized clinical trial platform and integrated product offerings that created the foundation for the company to realize 383% commercial growth. Castor now has more than 400 recurring paying customers, including a top-5 pharma company signed in Q1. 

On the early success of 2021, Castor CEO Derk Arts, MD, PhD, said “Historically, our products saw the strongest traction in the mid-market, but it’s clear that all segments are in need of a scalable, self-service platform to run more patient-centric trials. We are seeing growth in the big pharma segment ahead of our own plans, which is an indication of how COVID-19 accelerated the adoption of innovation.”

Looking forward, the company plans for 2021 to become the year in which they make decentralized trials scale, getting the technology in the hands of as many users as possible. Castor has a track-record in global study deployments, having supported more than 7,500 studies on its platform. The company will continue to deploy its suite of tools to enable enrollment, screening, and consenting in a fully remote or hybrid fashion. In parallel, the company’s mobile offerings are also expanding with the imminent release of its new ePRO app for iOS and Android.

Additionally, the company plans to capitalize on their investments in data standardization, by letting their first users experiment with digital twins: synthetic patients generated from metadata available from previous projects and the actual patients in the trial.

“For the future growth of Castor, it is instrumental that we keep looking for the best talent out there. We added more than 35 new hires to our ranks in the past four months, with a combined industry experience of more than 200 years,” said Derk. Castor’s new hires include the following:

Daniel Silva joins Castor’s Management team as VP of Customer Success and brings more than 20 years of experience in building customer success organizations at Oracle, TraceLink, and endpoint Clinical. “As a young technology company grows, it is crucial to have a scalable customer success model in place that can continue to provide customers with a superior overall experience,” said Dan. “Castor’s customers rate our products and services as one of the best in the eClinical industry*. I am excited to have the opportunity to continue to provide our customers with an outstanding experience as we double the number of customers in the coming year.” 

Senior Product Manager Sébastien Bohn brings more than 20 years of product management experience in the life sciences space at IBM, Merge Healthcare (acquired by IBM), and KIKA Medical International (acquired by Merge eClinical). “With Castor I see a massive opportunity to scale decentralized clinical trials for the first time, thanks to a technology-first approach, consisting of multiple native integrated product lines. This includes recruitment landing pages, enrollment, eConsent, EDC, reporting, and data analysis,” said Sébastien.

Director of Quality and Compliance Fatma Elfaghi brings more than 10 years of experience in managing compliance and regulatory affairs at Anju Software and OmniComm Systems. “It is amazing to see the foundation of Castor’s platform and the compliance procedures and documentation already in place that have resulted in successfully completed audits from major pharmaceutical companies,” said Fatma.

Castor is determined to hire more than 30 additional people in Q2 and Q3 to expand its global team.


About Castor 

Based in the United States and The Netherlands, Castor is an international health-tech company founded by CEO Derk Arts, MD, PhD. Their cloud-based clinical data platform simplifies the clinical trial process, from recruitment to analysis, for researchers worldwide.

More than 75,000 researchers across 90 countries are using Castor to supercharge their research. Castor’s platform has supported more than 7,500 commercial and academic studies that cover a broad range of therapeutic areas including diabetes, cardiovascular disease, rare diseases, infectious diseases, and oncology. Researchers on the platform generate vast amounts of data from traditional and remote trials, and Castor recently reached milestones of 250,000,000 data points and 2,500,000 enrolled patients. Castor’s goal is to make the world’s research data reusable, enabling AI-driven clinical trials, and ultimately creating a future in which they maximize the impact of data through reuse.

In 2020, Castor raised a $12M Series A from Two Sigma Ventures with participation from Hambrecht Ducera Growth Ventures and existing investor INKEF Capital. Castor previously raised a $6.25M seed round from INKEF Capital in 2018.

LinkedIn: www.linkedin.com/company/ciwit-b-v-
Twitter: www.twitter.com/castor


*Castor rated 4.7 out of 5 stars, from more than 100 customer reviews on Capterra.

Castor Provides Continued Support to the World Health Organization, Powering the World’s Largest Adaptive COVID-19 Trial

April 28th, 2021 by

HOBOKEN, NJ, UNITED STATES, April 28, 2021: Castor announces continued support to the WHO by powering the world’s largest adaptive COVID-19 trial: Solidarity.

Solidarity is an international clinical trial to help find an effective treatment among existing medications for COVID-19, launched by the World Health Organization and partners. It is one of the largest international randomized trials for COVID-19 treatments, having currently enrolled over 13,000 patients in 500 hospital sites in over 30 countries.

The Solidarity trial is evaluating the efficacy of drugs on three important outcomes in COVID-19 patients: mortality, need for assisted ventilation, and duration of hospital stay. Solidarity compares investigatory treatment options against standard-of-care to assess their effect on these three outcomes. Other drugs have been added to the trial continually, based on emerging evidence.

Castor is powering the WHO Solidarity trial with its remote and decentralized clinical research platform, along with 24/7 clinical support services. Castor rapidly deployed a clinical trial platform that successfully managed the complexities of a study conducted in over 30 countries, including offline capability for regions with poor internet connectivity.

The cornerstone of the Solidarity trial is its adaptive design born from necessity, as medication availability will vary by location, and as the WHO’s NEJM publication reported, additional therapies including monoclonal antibodies may be added.

According to the published paper, “The protocol was designed to involve hundreds of potentially over-stressed hospitals in dozens of countries,” making rapid and user-friendly data capture essential. “Online randomization and consent of patients [via Castor’s platform] took just a few minutes, as did online reporting of death in hospital or discharge alive.”

Spearheading the partnership for Castor, CEO Derk Arts, MD, PhD, said, “In the continued race against time to research effective COVID-19 treatments and vaccines, this trial has already enabled the world to reduce the number of patients admitted to ICUs and death from this disease.”

Arts continued, “At Castor, we strive to democratize clinical research through innovative clinical trial technologies, and ultimately create a future in which we maximize the impact of trials through increased patient access and diversity. Castor is proud to support the WHO in their critical efforts against COVID-19.”

About Castor
Castor is democratizing clinical trials with the highest rated eClinical platform for decentralized and hybrid clinical trials. Castor’s plug and play platform offers rapid deployment at scale, enabling researchers to create a trial in a matter of clicks, with easy enrollment and real-world data capture. Castor is bringing human-centered design to the clinical trial process, from recruitment to analysis, and improving the quality, security and reusability of data for researchers worldwide.

More than 75,000 researchers across 90 countries are using Castor to supercharge their clinical studies, enrolling more than 2.6 million patients. Castor’s platform has supported more than 7,500 studies around the world covering a broad range of disease areas including diabetes, cardiovascular disease, rare diseases, medical device and medical diagnostics. For more information, visit castoredc2.staging.wpengine.com

Doug Weatherhead
Castor
[email protected]

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Castor adds ISO 9001 to list of certifications

May 23rd, 2018 by

At the end of 2017, Castor became ISO 27001/27002 and NEN 7510 certified, which means we meet the highest standards for the protection of your data. Besides protecting your data, Castor also wants to deliver quality to its users across the board. That includes our product, our customer service and our operations. Therefore, our goal for this year was to become ISO 9001 (Quality) certified by April. ISO 9001 is an international standard for quality management and can be used to assess whether the organization is capable of meeting the requirements of customers, the applicable laws and regulations, and the requirements of the organization itself.

We have achieved our goal and are proud to announce that Castor is now adding ISO 9001 to our list of certifications! For more information on our compliance and certifications, read our security statement.

Castor Announces Partnership With Click Therapeutics to Support Decentralized Clinical Trials

August 31st, 2020 by

Hoboken, New Jersey: September 2, 2020: Castor, a leading provider of clinical trial technology that automates the research process, today announced its partnership with Click Therapeutics, a leader in the field of digital therapeutics, to provide solutions for conducting fully remote clinical trials.

Click Therapeutics develops and commercializes software as prescription medical treatments for patients with unmet medical needs. Click’s first marketed product, a digital program for smoking cessation is available to consumers through a variety of payers, providers, and employers. The company is also progressing a pipeline of prescription digital treatments across multiple indications, including for the treatment of depression, insomnia, acute coronary syndrome, migraine, overactive bladder, chronic low back pain, and obesity.

Castor will provide Click with solutions for digital enrollment, electronic consent (eConsent), and remote data capture (EDC and eCOA). By supporting a decentralized approach to research, the companies expect to reduce traditional trial duration and costs by at least 30 percent compared to conventional trial methods.

Spearheading the partnership, Castor CEO Derk Arts, MD, PhD, said, “I’m particularly excited about this opportunity because digital therapeutics are a key growth area for the industry. This, combined with the fully remote approach for Click’s clinical trials adds to my excitement, because supporting research that puts minimal strain on participants and investigators has always been a priority for Castor. We will accomplish this by allowing patients to enroll and consent into this study from anywhere in the United States, and capturing data on their progress remotely. It’s truly amazing to be able to support such a forward thinking company as Click Therapeutics.”

According to Cathleen Platt, Click’s Vice President of Clinical Development, “When selecting a partner for these upcoming trials, we compared traditional providers in the space with some of the newer companies. After an extensive RFP process, we determined that Castor was a forward-thinking, cost-effective provider who could deliver all required components, including EDC. As pioneers in our field, we needed a partner that has a clear vision for the industry and is as interested as we are in transforming how therapies are developed and delivered.”

Since February, Castor has prioritized supporting COVID-19 trials and developing decentralized clinical trial technology to enable vital research during the pandemic. Decentralized and hybrid clinical trials require fewer clinic visits and reduce the burden on patients and caregivers. Castor’s new video-enabled enrollment and eConsent platform can be combined with traditional eClinical components, such as EDC and ePRO, to allow investigators and participants to decide how and where they contribute to research. Castor’s partnership with Click will advance their common goal of making the clinical trial process more impactful, efficient, and patient-centric.

Castor decentralized trials APIAbout Castor 

Based in the United States and The Netherlands, Castor is an international health-tech company founded by CEO Derk Arts, MD, PhD. Their cloud-based clinical data platform simplifies the clinical trial process, from recruitment to analysis, for researchers worldwide.

More than 50,000 researchers across 90 countries are using Castor to supercharge their research. Castor’s platform has supported more than 4,000 commercial and academic studies that cover a broad range of therapeutic areas including diabetes, cardiovascular disease, rare diseases, infectious diseases, and oncology. Researchers on the platform generate vast amounts of data from traditional and remote trials, and Castor recently reached milestones of 180,000,000 data points and 2,000,000 enrolled patients. Castor’s goal is to make the world’s research data reusable, enabling AI-driven clinical trials, and ultimately creating a future in which they maximize the impact of data through reuse.

In 2020, Castor raised a $12M Series A from Two Sigma Ventures with participation from Hambrecht Ducera Growth Ventures and existing investor INKEF Capital. Castor previously raised a $6.25M seed round from INKEF Capital in 2018.

Castor provides free access to data capture platform to support COVID-19 research projects

February 17th, 2020 by

Amsterdam, Netherlands and Hoboken, New Jersey:  February 17, 2020: Castor, a health-tech company that enables medical researchers to capture standardized data to support data driven medical decision making, announced that it will provide free access to its data capture system to all COVID-19 research projects.

On January 30, 2020, the World Health Organization (WHO) declared the new airborne contagious coronavirus (SARS-CoV-2 a.k.a 2019-nCoV), that causes the disease dubbed COVID-19, a Public Health Emergency of International Concern. The WHO is providing technical guidance on how to conduct useful early investigations and has highlighted the need to assemble large amounts of accurate and usable data as quickly as possible.

Castor has developed and made available ready-for-use electronic Case Report Forms (eCRFs) based on the WHO standard CRFs, to help researchers start their study or registry in less than an hour, ensuring they capture high quality data to help drive the global research effort.

By ensuring researchers capture standardized data on Castor’s clinical data platform, clinical data from around the world can be easily aggregated. This approach can accelerate the work of researchers who are trying to understand the virus and disease. 

Commenting on the initiative, Castor’s CEO Derk Arts, MD, PhD, said: “When novel strains of viruses like the Coronavirus emerge, data quickly becomes our most valuable asset. On behalf of the team, I am proud to announce that Castor is joining the fight against COVID-19 by making our data capture platform available for free for all COVID-19 research projects.

“A standardized approach in collecting clinical data is critical in order  to better understand the natural history of disease and describe clinical phenotypes and treatment interventions (i.e. clinical characterization). For a global data collection effort to be truly successful, we need to go beyond standardized forms. The threshold for capturing these datasets should be as low as possible, to ensure anyone is willing and able to contribute valuable data.”

Castor encourages all COVID-19 researchers in need of standardized, high quality data to submit for a free billing code via [email protected], to start their studies by registering here, and to visit their online academy to become familiar with the platform. The WHO-defined CRFs can be downloaded here.

Castor’s Electronic Data Capture (EDC) system enables every researcher worldwide to easily capture and integrate medical research data from any source in real-time, including clinicians, patients, devices and wearables. Researchers on the platform generate vast amounts of data from traditional and decentralized trials, and Castor recently reached milestones of 130,000,000 data points and 1,400,000 enrolled patients.

ENDS 

For more information about Castor please contact:

Castor
John Ambrose, Esq
Head of Marketing
[email protected]

Media & IR Enquiries
Optimum Strategic Communications 
Mary Clark/ Hollie Vile/Manel Mateus
[email protected]

Tel: +44 (0) 20 3922 1906

NOTES TO EDITORS

About Castor 

Based in Amsterdam, The Netherlands and New Jersey, US, Castor is an international health-tech company founded by CEO Derk Arts, MD, PhD to leverage machine readable data to increase clinical trial efficiency. Castor’s Electronic Data Capture (EDC) system enables every researcher worldwide to easily capture and integrate medical research data from any source in real-time, including clinicians, patients, devices, wearables, and EHR systems.

More than 37,000 researchers across 90 countries are using Castor to supercharge their research. Castor’s platform has supported more than 4,000 commercial and academic studies that cover a broad range of disease areas including diabetes, cardiovascular disease, rare diseases, and oncology. Researchers on the platform generate vast amounts of data from traditional and decentralized trials, and Castor recently reached milestones of 130,000,000 data points and 1,400,000 enrolled patients. Castor’s goal is to make the world’s research data reusable, enabling AI-driven clinical trials, and ultimately creating a future in which they maximize the impact of data through reuse.

In 2018 Castor raised $6.25m in funding from early-stage investor INKEF Capital in the Netherlands.

Website: castoredc2.staging.wpengine.com

Twitter: @Castor

LinkedIn: linkedin.com/company/ciwit-b-v-

Castor Launches Scalable Decentralized Trial Platform After 383% Commercial Growth

December 17th, 2020 by

Hoboken, New Jersey: December 17, 2020: Castor, a leading provider of clinical trial technology, today announced the launch of its scalable end-to-end decentralized clinical trial (DCT) platform.

With this launch, Castor is meeting the increasing demand in the market for technology that makes trials more patient centric and enables a hybrid approach (in-home or site-based) to trial visits, which has been accelerated by the pandemic. The platform includes modules to support remote enrollment, remote eConsent, native patient-facing apps, a complete EDC, and integrated real-time reporting capabilities. 

On launching the DCT platform, Castor CEO Derk Arts, MD, PhD, said: “Castor has always had a strong focus on patient-centric and technology-enabled trials, as I believe these trials will become the reference standard for the life sciences industry. In the past nine months we focused our product development on creating a platform that makes these trials scalable, as we see an enormous bottleneck in the industry on launching these technologically challenging trials in acceptable timelines.”

The launch comes on the back of a high impact year for Castor, in which they supported the World Health Organization with their landmark Solidarity trials on COVID vaccines and treatments, and supported more than 300 COVID-related trials pro bono. In the second half of the year, commercial growth was 383% compared to the same period in 2019. A major commercial milestone was winning a contract for multiple cross-country eConsent projects with a top 10 pharma company.

Castor will be working closely with the recently launched Decentralized Trials & Research Alliance (DTRA) as one of the founding members to ensure the successful adoption of this technology.

Craig Lipset, DTRA Co-Convener and Castor Advisory Board member, said: “The pandemic has catalyzed the adoption of decentralized clinical trials, and sponsors are increasingly making it clear that there is no going back. While many embraced flexible participation as a necessity for business continuity, they are committing to these approaches to improve patient access, experience, and diversity.”

Castor’s key achievements in 2020 include:

About Castor 

Based in the United States and The Netherlands, Castor is an international health-tech company founded by CEO Derk Arts, MD, PhD. Their cloud-based clinical data platform simplifies the clinical trial process, from recruitment to analysis, for researchers worldwide.

More than 65,000 researchers across 90 countries are using Castor to supercharge their research. Castor’s platform has supported more than 4,000 commercial and academic studies that cover a broad range of therapeutic areas including diabetes, cardiovascular disease, rare diseases, infectious diseases, and oncology. Researchers on the platform generate vast amounts of data from traditional and remote trials, and Castor recently reached milestones of 250,000,000 data points and 2,200,000 enrolled patients. Castor’s goal is to make the world’s research data reusable, enabling AI-driven clinical trials, and ultimately creating a future in which they maximize the impact of data through reuse.

In 2020, Castor raised a $12M Series A from Two Sigma Ventures with participation from Hambrecht Ducera Growth Ventures and existing investor INKEF Capital. Castor previously raised a $6.25M seed round from INKEF Capital in 2018.

LinkedIn: www.linkedin.com/company/ciwit-b-v-
Twitter: www.twitter.com/castor

Castor Expands Platform Capabilities, Releases Virtual Visit Feature to Optimize the Clinical Trial Experience for Researchers and Patients

October 31st, 2022 by

NEW YORK, N.Y. – November 1, 2022 – Castor, a leading provider of decentralized and hybrid clinical trial solutions, today announced the release of Virtual Visits, a new telemedicine feature designed to enable faster, more diverse clinical trials. Seamlessly built into the company’s modular clinical trial platform, the newest release unites data capture with face-to-face interaction by connecting with patients in the comfort of their own homes, on any device.

“We’re thrilled to add Virtual Visits to our platform,” said Derk Arts M.D, Ph.D, Castor CEO and Co-Founder. “Our goal is to make clinical trials easier for everyone involved, whether that’s a researcher managing multiple studies or a participant juggling daily life commitments. This new feature allows us to continue moving towards that goal.”

By reducing the effort, cost, and time needed, Castor Virtual Visits enhance convenience and flexibility – upgrading the patient experience while also amplifying retention rates and data reliability. With Castor, patients can remotely connect with investigators or study coordinators on any device they want, in their preferred language – giving them the power to make informed decisions about their care.

Castor Virtual Visits facilitate direct data collection, making data quality, management, and sharing easier for clinical research teams. Researchers can conduct virtual visits through Castor’s EDC module, allowing for direct data capture to happen during virtual visits. Designed to ensure compliance with regulatory requirements, Castor’s secure telemedicine solution is fully compliant with regulations such as HIPAA and GDPR, ensuring patient privacy and data security.

With this expansion, Castor now has functionality for each major step of the clinical workflow. In addition to virtual visits, Castor’s modular clinical trial platform also offers patient engagement tools, electronic informed consent capabilities, and real-time data management. Together, these features streamline clinical trial workflows while improving the clinical trial experience for all stakeholders involved.

Castor continues to innovate in the clinical trial space, driving toward more efficient and accessible research. To learn more about Virtual Visits and the rest of Castor’s platform, visit www.castoredc.com.

About Castor

Castor is a leading provider of decentralized and hybrid clinical trial solutions to democratize research. With the highest-rated eClinical platform, Castor’s modular platform offers rapid deployment at scale, enabling researchers to create a trial in a matter of clicks, with easy enrollment and real-world data capture. Castor is bringing human-centered design to the clinical trial process, from recruitment to monitoring, and improving the quality, security, and reusability of data for researchers worldwide. For more information, visit www.castoredc.com. Follow Castor on LinkedIn or Twitter.

Contacts

Castor
Dana Perotti, [email protected]

Media
KKH Advisors
Kimberly Ha,
[email protected]

Castor announces Frans van Houten, former CEO of Philips, as the company’s new chairman of its Board Of Directors

August 21st, 2023 by

NEW YORK, N.Y. – August 21, 2023 – Castor, an industry leader in modular, patient-centric, clinical trial technology, today announced the appointment of Frans van Houten as the new Chairman of its Board of Directors. His exceptional leadership experience and extensive industry knowledge in the healthcare and technology industries will be invaluable to Castor as the company continues to pursue its mission to make patient-centric trials possible for everyone, anywhere in the world.

Frans van Houten, recognized worldwide for his tenure as CEO of Philips, contributes a proven track record in business transformation, and technology innovation. During his tenure at Philips, he was responsible for transforming the organization from a diversified conglomerate into a focused health technology solutions company. Aside from his role at Castor, van Houten also serves on the Board of Directors of Novartis, a leading global pharmaceutical company, and acts as a key advisor to private equity companies. 

“Efficient clinical trials produce quality data that need to be collected through effective engagement with patients, processed and aggregated, all responsibly in compliance with regulatory requirements,” said van Houten. “I have long shared Castor’s belief that clinical trial cloud technology can do a better job in helping pharmaceutical and biotechnology companies scale and expedite timelines with more data accessibility. By combining clinical trial expertise with modern SAAS technology, we will be able to fix traditionally stodgy clinical trial processes to increase operational efficiencies and reduce human effort at every stage in the clinical trial journey.” 

“Being able to work with a renowned captain of industry and thought leader such as Frans is a true privilege. I am excited to work with him to ensure Castor stays ahead of our peers with regards to innovation and growth.”  said Derk Arts, MD, PhD, CEO and Founder of Castor. “His expansive expertise in the life science and healthcare informatics industries will not only accelerate our growth as we partner with enterprise pharma, but also ensure we effectively navigate these times of drastic change with the advent of AI in clinical research.”

About Castor

Castor is a leading provider of decentralized and hybrid clinical trial solutions to democratize research. With the highest-rated eClinical platform for decentralized and hybrid clinical trials, Castor’s plug-and-play platform offers rapid deployment at scale, enabling researchers to create a trial in a matter of clicks, with easy enrollment, consent, and real-world data capture. 

Castor is bringing human-centered design to the clinical trial process, from recruitment to analysis, and improving the quality, security, and reusability of data for researchers worldwide. 

For more information, visit www.castoredc.com. Follow us on LinkedIn at https://www.linkedin.com/company/castoredc

 

Contact
Laura McLoughlin
Castor
[email protected]

Castor announces appointment of Brad Hightower, leading clinical trials executive, to its advisory board

February 1st, 2023 by

NEW YORK, N.Y. – February 1, 2023 – Castor, a leading provider of clinical trial technology to democratize clinical research, today announced the appointment of Brad Hightower, a leading clinical trials executive, to its advisory board.

Brad brings more than 10 years of experience in clinical research, as the former Executive Director of the Oklahoma Heart Hospital Research Foundation. He founded Hightower Clinical, a research network that offers services that support researchers and patients to access trials easily.

“I am excited to join Castor’s Advisory Board,” said Brad Hightower. “I have been a fierce advocate for patients’ access and seeing little changes in how we conduct trials that truly benefit our patient population. I believe in the potential of technology to fill in this gap. Castor is bringing the right technology to connect patients and study teams.”

About Castor

Castor is a leading provider of decentralized and hybrid clinical trial solutions to democratize research. With the highest-rated eClinical platform for decentralized and hybrid clinical trials, Castor’s plug-and-play platform offers rapid deployment at scale, enabling researchers to create a trial in a matter of clicks, with easy enrollment, consent, and real-world data capture. Castor is bringing human-centered design to the clinical trial process, from recruitment to analysis, and improving the quality, security, and reusability of data for researchers worldwide.

For more information, visit www.castoredc.com. Follow Castor on LinkedIn or Twitter.

Contacts

Castor
Laura McLoughlin, [email protected]

Media
KKH Advisors
Kimberly Ha,
[email protected]

Castor Introduces Castor CoPilot, A Novel AI Solution for Clinical Trials

June 12th, 2024 by

Castor Research Inc, New York City – June 13, 2024 – Castor, a leader in clinical trial technology solutions, today announced the launch of Castor CoPilot, an innovative human-in-the-loop AI tool designed to replace manual data re-entry and source data verification (SDV) processes in clinical trials. This cutting-edge solution is set to debut at the DIA Global Global Annual Meeting 2024 in San Diego, with a live demonstration by CEO Derk Arts, on Innovation Theater #3 at 12.15pm on Monday, June 17th.

Castor CoPilot employs advanced AI to automate and streamline data collection traditionally performed manually, thereby reducing the time required for data entry by up to 70% and eliminating the need for source data verification. The capability integrates seamlessly into existing workflows, supports risk-based monitoring, and is capable of being deployed in ongoing studies with minimal disruption.

Advancements and Collaborations:

As part of its Practical AI roadmap, Castor has previously launched the AI Study Builder and now introduces Castor CoPilot as its second major AI capability. These developments reflect Castor’s strategic use of technology to minimize manual work and enhance trial efficiency. Furthermore, Castor’s collaboration with Microsoft has been instrumental in leveraging cloud computing and AI technologies to support these innovations, ensuring scalability and security across its platform.

Impact on Clinical Research:

“The introduction of Castor CoPilot is a significant step forward in our mission to reduce repetitive, expensive and unfulfilling work in clinical trials that is burning out site staff” stated Dr. Derk Arts, CEO of Castor. “Our CoPilot is taking aim at the real problems in Clinical Research: lack of site staff and exploding site burden. A problem that will only get exacerbated by the hype around AI drug discovery.”

Castor CoPilot, seeks to reduce high turnover rates among site staff and clinical research associates by reducing the repetitiveness of day to day tasks, leading to improved job satisfaction and retention within the field. Its deployment is expected to increase operational margins by reducing the need for extensive manual data handling.

Castor has announced it will open a waitlist for interested sponsors looking to reduce burden in, initially, real-world-evidence studies. 

About Castor:

Castor is at the forefront of transforming clinical trials through practical applications of AI and innovative data solutions. Committed to advancing medical research, Castor leverages its technology to automate complex processes, prioritize patient safety, and comply with regulations. With a focus on AI development, including collaborations with major technology providers like Microsoft, Castor is dedicated to improving the clinical trial experience and outcomes.

For More Information:

Join the waitlist for Castor CoPilot HERE.

Laura McLoughlin

[email protected]

Follow us on LinkedIn: Castor | Derk Arts

Castor receives ISO 27001 certification

December 20th, 2017 by

Castor is now ISO 27001 certified!

As of November 2017, Castor is officially certified in the field of Information Security (ISO 27001 – Standards for Information Security Assurance), the standard that describes how Information Security should be organized in a process-based manner in the context of the general business risks for the organization.

Information Security plays an increasing role in international organizations, due to the increase of external risks. At Castor, we process highly sensitive information and thus we need to have all information security procedures in order. An independent auditor assessed Castor very positively, without a single deviation. Castor complies with the international standard for securing systems containing information. This ensures the data of our customers and protects medical data in a standardized way.

Castor is also NEN 7510 (Dutch Standardization Institute) certified. This is the Dutch Standard for Healthcare Information Security and proves that Castor handles medical research data with the utmost care, security and responsibility.

Would you like to know more about our quality and information security management system (QISMS) or certification? Please contact our QISMS coordinator, Veroni Smidt-Verhulst.

HealthVerity and Castor launch partnership to seamlessly incorporate real-world data throughout the clinical trial lifecycle

July 2nd, 2024 by

Synchronizing state-of-the-art eConsent platform with the nation’s largest fully interoperable and research-ready data ecosystem to advance the science

Philadelphia, PA and New York, NY – 30th May, 2024 – HealthVerity, the leader in synchronizing transformational technologies and real-world data (RWD) to advance the science, and Castor, a leading provider of decentralized and hybrid clinical trial solutions, today announced a strategic partnership to streamline the synchronization of clinical trial and real-world data throughout the clinical research stages.

This patient-centric solution uses Castor’s all-in-one eConsent platform to seamlessly capture patient consent and the personally identifiable information (PII) needed to de-identify patients and synchronize them to their RWD without any additional burden on clinical trial sites, even managing re-consents as needed. The customizable and flexible platform educates patients on how their RWD will be used and their privacy protected, allowing the patient to easily manage their informed consent. 

Once consent and PII is captured, HealthVerity Identity Manager assigns trial participants a universal identifier or token, known as a HealthVerity ID (HVID), which serves as a single source of truth, allowing researchers to easily discover and match patient’s to their RWD across sources, synchronizing it with clinical trial data in a fully HIPAA-compliant and privacy certified manner. 

This process makes clinical trial participants instantly interoperable with the nation’s largest healthcare and consumer data ecosystem and HealthVerity Marketplace, where investigators can explore novel RWD sources and build custom patient cohorts in real time to discover and exchange transaction-level, research-ready RWD with ease. 

This end-to-end solution allows investigators to continue to track patient permissions to ensure compliance and be able to leverage research-ready RWD at any time throughout the clinical trial to:  

“This partnership empowers life science organizations to realize the full potential of real-world data and generate the real-world evidence needed to advance healthcare,” said Andrew Kress, HealthVerity CEO.

“It also enhances our patient journey software solution, HealthVerity FLOW, a modular 21 CFR 11-certified SaaS solution that offers unparalleled patient identity resolution, while maintaining privacy compliance and governing patient permissions and data usage rights for the efficient discovery and exchange of a near limitless combination of real-world data at a record pace.”

About HealthVerity

HealthVerity synchronizes transformational technologies with the nation’s largest healthcare and consumer data ecosystem to power previously unattainable outcomes and fundamentally advance the science. We offer a comprehensive, yet flexible approach, based on the foundational elements of Identity, Privacy, Governance and Exchange (IPGE), that synchronizes unparalleled Identity management with built-in Privacy compliance and Governance, providing the ability to discover and Exchange a near limitless combination of data at a record pace. Together with our partners in life sciences, government and insurance, we are Synchronizing the Science. To learn more about HealthVerity, visit healthverity.com.

About Castor

Castor is dedicated to making a lasting impact on evidence-based medicine with our innovative, patient-centric clinical trial platform. With human-centered design we enable researchers to conduct global, inclusive and diverse clinical trials. Castor leverages an API-first approach to ensure efficient study data collection and integration of complex real world data sets. With our plug-and-play modules researchers can effortlessly launch a trial with just a few clicks. Our robust, cloud-native platform guarantees maximum security and scalability, providing reliable service delivery. 

Ultimately, our vision is to improve health equity and extend the human healthspan by revolutionizing clinical trials.

 

Castor Contact:
Laura McLoughlin
[email protected]
Follow us on LinkedIn: Castor | Derk Arts

HealthVerity Contact:
Colleen Stoker
[email protected]

Castor launches COVID-19 monitoring and research platform, and is supporting over 100 trials globally

April 2nd, 2020 by

Platform to facilitate rapid deployment of trials to test vaccines and treatments

 

Hoboken, New Jersey: April 2, 2020: Castor, a health-tech company that enables medical researchers to capture machine readable data to optimize medical decision making, announced the launch of its global COVID-19 monitoring and research platform to facilitate the rapid deployment of trials to test Coronavirus vaccines and COVID-19 treatments. After offering free access to their platform for all COVID-19 research projects in mid-February, Castor is now supporting over 100 studies. 

Castor’s platform includes an online enrollment portal for patients, an eConsent module, and a Symptom Tracker app, all integrated with Castor’s Electronic Data Capture (EDC) system. This platform is freely available for everyone fighting COVID-19, including biotechnology and pharmaceutical companies. The platform was designed to be rapidly configured and deployed.

Following easy online enrollment and eConsent, patients are randomized in the EDC. Depending on country protocols, vaccines can then be shipped to enrolled subjects and administered in their homes. In addition, real-time dashboards enable study personnel to monitor the population and proactively reach out to patients who are showing symptoms of COVID-19. These patients could then be enrolled in further interventional studies or triaged in a hospital.

Launching the platform, Castor CEO Derk Arts, MD, PhD, said: “High-quality data and real-time access are critical in the fight against the COVID-19 pandemic. We are proud to support the global research effort by launching a mobile-enabled solution that allows decentralized patient participation and remote monitoring of study participants. This will help reduce hospital crowding, protect staff, and prioritize patients that need to be hospitalized.”   

Craig Serra, Global Head of Strategy and Innovation, Data Operations at Novartis, and Castor Advisory Board member, added: “With increased disruption to clinical trials, it is essential for medical research to adopt methods for remote engagement and monitoring, outside of a clinical setting. Now is the time, more than ever, to stop talking about solutions and take action on them.”

Alongside this platform, Castor is supporting research into the disease by providing free access to their research data platform for all COVID-19 studies. By enabling large-scale decentralized trials, Castor aims to accelerate the work of researchers who are trying to combat the disease. Castor is currently supporting more than 100 COVID-19 studies across 10 countries. This includes research projects at the University Hospital Southampton in the UK, Policlinico Universitario A. Gemelli in Italy, Vall d’Hebron Research Institute in Spain, and UMC Utrecht in the Netherlands.  

Denise Van Hout, MD, an Epidemiologist and member of the team at UMC Utrecht using Castor to study COVID-19 preparedness of healthcare workers, added: “In the race to understand and develop treatments and vaccines for this disease, Castor’s platform is making a difference by supporting free research projects that can be rapidly built and deployed.”  
 
For more information about Castor and the COVID-19 monitoring and research platform please contact:

Castor

COVID-19 support team
[email protected]

John Ambrose, Esq
Head of Marketing
[email protected]


Media & IR Enquiries

Optimum Strategic Communications 

Mary Clark/ Hollie Vile/Manel Mateus
[email protected]
Tel: +44 (0) 20 3922 1906


NOTES TO EDITORS

About Castor 

Based in Amsterdam, The Netherlands and New Jersey, US, Castor is an international health-tech company founded by CEO Derk Arts, MD, PhD to leverage machine readable data to increase clinical trial efficiency. Castor’s Electronic Data Capture (EDC) system enables every researcher worldwide to easily capture and integrate medical research data from any source in real-time, including clinicians, patients, devices, wearables, and EHR systems.

More than 40,000 researchers across 90 countries are using Castor to supercharge their research. Castor’s platform has supported more than 4,100 commercial and academic studies that cover a broad range of disease areas including diabetes, cardiovascular disease, rare diseases, infectious diseases, and oncology. Researchers on the platform generate vast amounts of data from traditional and decentralized trials, and Castor recently reached milestones of 140,000,000 data points and 1,500,000 enrolled patients. Castor’s goal is to make the world’s research data reusable, enabling AI-driven clinical trials, and ultimately creating a future in which they maximize the impact of data through reuse.

In 2018 Castor raised $6.25m in funding from early-stage investor INKEF Capital in the Netherlands.

Castor encourages all COVID-19 researchers in need of standardized, high quality data to start their studies by registering here, and to visit their online academy to become familiar with the platform. The WHO-defined CRFs can be downloaded here.

Castor Launches “Castor for Impact Program” to Advance Health Equity in Clinical Research

August 12th, 2024 by

Innovative Program Offers Discounted or Free Access to Clinical Trial Technology, Empowering Underserved Research Areas and Early-Stage Biotech and Medical Device Companies

New York, NY – 12th August, 2024 – Castor, a leading provider of clinical trial technology solutions, today announced the launch of its “Castor for Impact Program“. This initiative offers discounted or free access to Castor’s Essentials clinical trial technology package (consisting of Electronic Data Capture (EDC), web-based Electronic Patient Reported Outcomes (ePRO), and online training and support) for eligible institutions and businesses, aiming to enhance health equity and extend human health span.

The Castor for Impact Program targets organizations conducting research in Preventive Medicine, neglected tropical diseases, public health issues in underserved communities, women’s health, and ultra-rare diseases. It also supports academic institutions running trials with limited funding and smaller, early-stage biotech and medical device companies that need to run cost-effective trials.

Bridging the Gap in Clinical Research:

“After supporting 100s of COVID studies pro-bono, it was time to broaden our scope and leverage Castor’s platform to support all communities and innovations that need help fighting the global disease burden,” said Dr. Derk Arts, CEO of Castor. “The Castor for Impact Program is our commitment to making evidence-based medicine more accessible.”

This program contributes directly to Castor’s vision of extending the human health span and increasing health equity through innovative technology and effective data utilization. By providing access to advanced clinical trial tools, Castor aims to accelerate research in underserved areas and democratize access to cutting-edge technology.

Key Features of the Program:

Impact on Clinical Research:

The Castor for Impact Program is expected to significantly reduce barriers to entry for crucial research projects that often struggle with funding and resources. By providing access to Castor’s technology, the program aims to improve data collection, management, and analysis capabilities for these vital studies.

Interested organizations can check their eligibility and apply for the program through the Castor website.

About Castor:

Castor is dedicated to advancing medical research by empowering researchers with high-quality, user-friendly software. Our products include Castor EDC, Castor ePRO, Castor eCOA, Castor eConsent, and Castor SMS, each designed to enhance data collection, improve patient engagement, and ensure compliance with regulations.

Castor Contact:
Laura McLoughlin
[email protected]
Follow us on LinkedIn: Castor | Derk Arts

Castor welcomes Jeanne Hecht to Board of Directors

July 3rd, 2023 by

NEW YORK, N.Y. – July 5, 2023 – Castor, an industry leader in modular, patient-centric, clinical trial technology, today announced the appointment of Jeanne Hecht to its Board of Directors. She will contribute extensive experience and strategic insights to support Castor’s mission of making patient-centric trials possible for everyone, anywhere in the world.

“The clinical trial landscape requires collaboration among key stakeholders,” said Hecht. “To support the every changing needs of life science stakeholders including pharmaceutical companies, regulators, and research sites, innovation must occur. Castor’s modular platform is built to make clinical trials of varying size or complexity possible for everyone. I am eager to contribute my expertise and become a part of the company’s journey to make patient-centric trials possible for everyone, anywhere in the world.”

Jeanne Hecht, a Global Business Executive in the clinical research industry, has 25+ years of experience leading successful teams across mature and emerging markets within the product development, pharma services and life sciences space. Before joining Castor, she held multiple key roles at renowned life science organizations namely IQVIA, Median Technologies, and Ora where she held various executive leadership roles responsible for leading and implementing the companies’ global strategy. Her significant expertise in driving businesses will help Castor achieve breakthrough growth in key segments. 

“At Castor, we are breaking down silos and making it easier for everyone who is involved in the clinical trial processes,” said Derk Arts, MD, PhD, CEO and Founder of Castor. “Jeanne’s insights and enthusiasm for strategic business development combined with the collective experience of our leadership team and Board, will help facilitate collaboration and further our product positioning in the market.”

About Castor

Castor is a leading provider of decentralized and hybrid clinical trial solutions to democratize research. With the highest-rated eClinical platform for decentralized and hybrid clinical trials, Castor’s plug-and-play platform offers rapid deployment at scale, enabling researchers to create a trial in a matter of clicks, with easy enrollment, consent, and real-world data capture. 

Castor is bringing human-centered design to the clinical trial process, from recruitment to analysis, and improving the quality, security, and reusability of data for researchers worldwide. 

For more information, visit www.castoredc.com. Follow us on LinkedIn at https://www.linkedin.com/company/castoredc

Contact
Laura McLoughlin
Castor
[email protected]

Lightship Announces Partnership with Castor to Scale Virtual Clinical Trials Worldwide

June 24th, 2021 by

EL SEGUNDO, Calif. & HOBOKEN, N.J.

Lightship and Castor, leading providers of decentralized clinical trial solutions, today announced a strategic partnership to run direct-to-patient (hybrid) clinical trials at scale. The partnership combines operational excellence in clinical studies and technology that delivers for the most complex clinical trials.

For decades, clinical trials have experienced low rates of participation relative to the distribution of a condition, which can impact the ability to access diverse patient populations and construct a representative sample. One of the main reasons for this is the high burden of participation that patients often experience.

Lightship’s end-to-end delivery model combined with an in-house care team provide the best possible patient experience in clinical trials. By partnering with Castor’s proven, globally compliant Decentralized Clinical Trial and Clinical Data Management platform Lightship is strengthening its commitment to deploying best-in-class virtual tools. Lightship’s focus on the patient at every step, from recruitment through to study completion and beyond, is supported by the Lightship patient application.

Lightship and Castor will work in close collaboration on clinical studies, providing a seamless experience for physicians, nurses, and study coordinators. The partnership enhances the speed and simplicity of building clinical studies, data integration, and real-time reporting.

“For both Castor and Lightship, the patient experience comes before anything else. Together we’re improving access to clinical trials for a more diverse range of patients globally, and enhancing the process for patients and clinicians,” said Sam Eells, Co-Founder at Lightship.

“This partnership further strengthens Lightship’s end-to-end service by helping to manage studies even more efficiently, with easy-to-use digital health technologies.”

“Lightship provides world-class services that are critical to conducting successful decentralized and hybrid trials. They’re an excellent partner for Castor and share our vision as we advance towards scalable DCT solutions that democratize and increase access to clinical research,” said Derk Arts, M.D., Ph.D., Founder and CEO of Castor.

About Lightship

Lightship is the virtual-first provider that is perfecting the way clinical trials get done. Because clinical research plays such a vital role in bringing life-enhancing and life-saving innovations to market, Lightship pursues operational excellence in clinical studies. Our end-to-end delivery model, our diversity of skill sets, and in-house care team ensure sponsor success and the best possible patient experience. Learn more about us at www.lightship.com.

About Castor

Castor is Democratizing Clinical Research with the highest-rated eClinical platform for decentralized and hybrid clinical trials. Castor’s plug and play platform offers rapid deployment at scale, enabling researchers to create a trial in a matter of clicks, with easy enrollment and real-world data capture. Castor is bringing human-centered design to the clinical trial process, from recruitment to analysis, and improving the quality, security and reusability of data for researchers worldwide.

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