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 mitigate the impact on clinical trials while protecting participant safety.
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
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 critical during COVID-19 and beyond.
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 requirements.