Resource Library

Informed consent is a critical aspect of clinical trials. But what criteria must be met? And is there more than one type of consent? Find out here.

Castor’s Action Hours during Pride Month gave all Castorians the opportunity to educate themselves and celebrate the LGBTQIA+ culture.

The future of informed consent is digital. Learn about the benefits, the process, the regulatory landscape, and the future of eConsent here.

Lightship and Castor, leading providers of decentralized clinical trial solutions, today announced a strategic partnership to run direct-to-patient (hybrid) clinical trials at scale.

Learn key compliance requirements, data collection tips, and important dates for the EU Medical Device Regulation in this white paper.

May is Mental Health Awareness Month, and Castor initiated a conversation about well-being at work and mental health in general. Read more:

Castor is supporting more than 250 COVID-19 studies in 40 countries across 1,750 hospitals as it continues to grow its DCT platform.

Post-market surveillance (also known as Post-Marketing Surveillance or PMS) refers to the requirement that manufacturers monitor their medical…

We sat down with two of our Business Development Directors to find out what their work involves, why they are passionate about being Castorians, and a part of Castor’s purpose-driven mission.

Join this webinar and learn how to easily change, review and approve eCRF forms in your test environment, without impacting the production study.