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Castor Raises a $12M Series A to Further Their Support for COVID-19 Research
With 4,000 live studies and 2M enrolled patients across 90 countries, Castor will use the funding to further...
The Impact of ISO 14155 on PMCF Investigations Under the MDR
Download this white paper to prepare for the new MDR requirements requiring that PMCF investigations be conducted in...
An Expert Panel on Decentralized and Hybrid Trials, Pre and Post COVID-19
The world may have changed seemingly overnight, but clinical research and medical innovation must continue now more than...
How to build eCRFs to effectively set up your study
In this webinar, we discussed how to build your study form (eCRFs) on Castor EDC as well as...
5 Ways to Leverage Castor’s API for Better Clinical Trials
eClinical systems must be flexible and adaptable to keep up with the ever-changing demands of modern clinical trials....
A step-by-step tutorial on creating an approved PMCF plan
Under the MDR, PMCF activities will be mandated as part of medical device surveillance programs. These activities should...
What Will Trial Enrollment & Engagement Look Like in a Socially-Distanced World?
When the COVID-19 pandemic began, the industry needed to focus immediately on research continuity and determine how to...
Jumpstart Your Medical Device Preclinical Phase
The path to market for medical devices can be fraught with obstacles. One of the first challenges confronted...
The future of data standardization in medical research: FHIR and FAIR
Medical research data holds the key to solving the world’s greatest healthcare challenges. It is therefore, one of...
6 essential steps to ensure MDR compliance before May 2021
A recent report surveying representatives from the medical device industry across the world found that more than 55%...
How MedRhythms Captures Clinical Efficacy Data with Castor
MedRhythms used Castor's EDC and eCRF solutions to conduct their pivotal study. Castor's eCRF provides an instant snapshot...
Using Decentralized Trial Technology to Ensure Study Continuity and Data Quality During COVID-19 and Beyond
Download this white paper to learn why patient-centric, remote research technologies such as eConsent, EDC, and ePRO are...
How to manage your study in Castor
During this webinar, we showed how to efficiently manage studies in Castor. This includes: How to add users...
5 steps to meet PMCF requirements
Read the white paper to learn how Castor’s 5-step approach to PMCF can be used to fulfill MDR...
Tips & Tricks for data entry in Castor EDC
This webinar is dedicated to data entry users of Castor EDC. If you are conducting data entry for...
Satisfying PMCF requirements by utilizing IIS data
This white paper describes an approach that would enable medical device manufacturers to leverage anonymous data from IIS...
Protocol Deviations in Clinical Trials: Understanding the FDA’s Guidance
Protocol deviations can seriously impact the integrity of clinical trials, and with regulatory scrutiny growing, it’s crucial to...
All you need to know about randomization in Castor
This webinar teaches everything you need to know about randomization in Castor. This includes: How to randomize records...
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