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2023 Guide to Clinical Data Collection under the EU Medical Device Regulation (EU MDR)
Learn key compliance requirements, data collection tips, and important dates for the EU Medical Device Regulation in this...
AKRN handles mid-study changes in medical device clinical trials with Castor EDC
AKRN Scientific Consulting, a medical device CRO, used Castor's flexible EDC solution to handle constant mid-study changes for...
Automated data capture with eSource to train an AI algorithm
Castor’s eSource platform streamlined collecting, capturing & processing large amounts of clinical data to train AusculThing’s AI algorithm.
COVID-Red: Evaluating wearables for early remote COVID-19 detection & monitoring
When the pandemic hit, Julius Clinical was passionate to help in the global fight against COVID-19 and excited...
MedTech Methodology: Finding the right tech-enabled partner for your medical device trials
From pre-market trials to post-market observational studies, hear from industry experts as they review three different case studies...
Using APIs to enhance medical device data capture
Application programming interfaces (API) are an essential feature of any clinical technology platform, saving researchers time and money
How to Incorporate Remote Technology in Your Next Medical Device Trial
Researchers are looking to incorporate remote technologies into medical device trials for a wide range of device classifications....
Overview of EU Medical Device Regulations
Medical device regulations in the EU have recently undergone a major overhaul. Learn the key tenets of MDR...
How Medical Device Trials Can Benefit From Decentralized Methods
In this whitepaper, we will look at how EDC, eConsent, ePRO, and APIs enable researchers to easily conduct...
Castor is accelerating global medical device research with decentralized clinical trials platform
Castor’s DCT platform helping medical device trials achieve compliance with patient-focused technology Driving innovation for medical device clinical...
The Ultimate Guide to Post-Market Surveillance: What You Need to Know
In today’s rapidly evolving regulatory landscape, ensuring medical device safety and performance goes beyond the approval phase. Effective...
Essential Guide to Post-Market Clinical Follow-Up (PMCF) for Medical Devices
Learn the full impact of PMCF under the EU MDR and how to best prepare your medical device...
PMCF & RWE: Roles of Medical Device Registry Studies & ePROs
Registry studies focused on a specific medical device are a valuable tool to capture the safety and outcomes...
A Guide to Capturing and Managing Data in Digital Therapeutics Trials
This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote...
eBook: The Decentralized Clinical Trial Playbook
This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote...
UKCA Mark: 7 Steps to Prepare Medical Devices for Brexit
In the wake of Brexit, medical device companies secure a UKCA mark as proof of conformity to place...
Guide to using Electronic Data Capture (EDC) for Medical Device & Diagnostics Trials
Download this guide to learn how to incorporating an Electronic Data Capture (EDC) system in your medical or...
Common shortcomings of clinical research data for PMCF
The following is an excerpt from our free whitepaper ‘Satisfying PMCF requirements by utilizing IIS data’. Click here...
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