Three Ways Remote eConsent Improves Trial Efficiency
eConsent accelerates enrollment, increases retention, and reduces site burden. Learn why it’s the way of the future for clinical trials.
Video Conferencing for Remote eConsent: 5 Reasons to Make the Switch
Castor is using video conferencing to meet participant needs and lower site burden in clinical trials. Find 5 benefits here.
How to Prepare an IRB Submission for a Remote eConsent Study
If you are planning on using eConsent in a trial, you’ll need to include it in your IRB submission. Find out what to include here.
Understanding the Nuances of Informed Consent in Clinical Trials
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.
Putting PRIDE Into Action at Castor
Castor’s Action Hours during Pride Month gave all Castorians the opportunity to educate themselves and celebrate the LGBTQIA+ culture.
The True Meaning & Value of eConsent in Clinical Trials
The future of informed consent is digital. Learn about the benefits, the process, the regulatory landscape, and the future of eConsent here.
Putting Well-Being First: How Castor Promotes a Happy and Healthy Team
May is Mental Health Awareness Month, and Castor initiated a conversation about well-being at work and mental health in general. Read more:
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…
A day in the life of a Director, Business Development at Castor
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.
