Women in Technology: Castor Interview Series 3 – Luciana Mendonça
Our Women in Technology series continues with Luciana Mendonça, Software Engineer.
Women in Technology: Castor Interview Series 2 – Elena Tanturovska
Our Women in Technology series continues with Elena Tanturovska, QA Automation Engineer.
RWE and PMCF: The Role of Registry Studies and PROs
Registry studies focused on a specific medical device are a valuable tool to capture the safety and outcomes of the device over its lifetime. Read more here.
Castor Inks Big Pharma Deal As Decentralized Trials Business Continues to Show Exponential Growth
Hoboken, New Jersey: March 10, 2021: Castor, a leading provider of clinical trial technology, today announced the signing…
Essential 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 white paper.
Women in technology: Castor Interview Series, Roxana Cristian
In the Castor D&I interview series, Castorian women in technology share their experiences and thoughts on making the workplace more inclusive.
Launching a “Remote-first” Universe: Practical Tips from Castor
Castor’s most significant core value is “Achieve anything with a happy and healthy Team,” and so we wanted to ensure we embrace this value even more in a remote-first set-up where employees are not regularly coming into a shared working space.
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 interactions in their clinical studies.
Why Remote Consent Is the New Normal in 2021
COVID-19 changed the conversation around enrollment and recruitment for clinical trials. Learn how eConsent is helping researchers do more despite restrictions.