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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...
In-Vitro Diagnostic Regulation (IVDR): From oversight to overhead
The rising demand for early, accurate disease diagnosis and the growing possibilities in personalised medicine are driving the...
How to effectively monitor studies in Castor EDC
This webinar covers everything you need to know about monitoring in Castor. This includes: Raising and managing queries...
Castor vs. the Coronavirus and COVID-19
Last updated on June 30, 2020 For existing and new Castor customers Castor will continue to deliver its...
6 essential steps to ensure Medical Device Regulation (MDR) compliance before May 2021
July 17th 2020: This document has been updated to reflect regulatory changes in response to COVID-19. As this...
How to create patient surveys in Castor (ePRO/eCOA)
In this webinar, we teach how to send questionnaires / electronic patient-reported outcomes (ePRO) to patients that will...
What does the Medical Device Regulation (MDR) tell us about Post-Market Surveillance?
With the Medical Device Regulation (MDR) coming into full force in 2020, medical device companies should prepare for...
An Engineering Spotlight: What’s it like to ‘crunch the code’ at Castor?
Bas is one of our Senior Software Engineers. Having recently joined our team of Castorians, I wondered how...
Three expected changes to FDA medical device approval
2019 was an interesting year for medical device companies. In our previous blog articles, we discussed the complete overhaul...
Impact of ISO 14155 on PMCF Investigations Under the MDR
Through the Medical Device Regulation (MDR) and new version of ISO 14155, the regulatory landscape for clinical investigations with...
Impact of COVID-19 and the Imminent MDR Delay
Introduction The implementation of the new EU Medical Device Regulation (MDR) just got a plot twist: COVID-19. This...
Using Machine Learning to Identify At-Risk COVID-19 Patients (COVID-PREDICT)
The ongoing COVID-19 pandemic is one of the most serious health crises in modern history, affecting an unprecedented...
4 ways the Medical Device Regulation (MDR) will impact your device studies
Medical device companies targeting the EU market are being confronted with significant regulatory changes for market access. As...
Mitigating the impact of COVID-19 on clinical research
Clinical trials are experiencing significant disruption worldwide due to the COVID-19 pandemic. Medical research is not immune to...
Forecasting the impact of COVID-19 on medical device trials
As of early April 2020, over 1,000,000 people have been confirmed infected with the SARS-CoV-2 coronavirus, and governments...
Castor launches COVID-19 monitoring and research platform, and is supporting over 100 trials globally
Platform to facilitate rapid deployment of trials to test vaccines and treatments Hoboken, New Jersey: April 2,...
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