What Is eConsent in Clinical Trials?
eConsent accelerates enrollment, increases retention, and reduces site burden. Find out why it’s the way of the future for clinical trials here.
eConsent accelerates enrollment, increases retention, and reduces site burden. Find out why it’s the way of the future for clinical trials here.
Castor and Lightship discuss the infrastructure needs for providing the best patient experience and ensuring data integrity in decentralized clinical trials.
eConsent accelerates enrollment, increases retention, and reduces site burden. Learn why it’s the way of the future for clinical trials.
Castor is using video conferencing to meet participant needs and lower site burden in clinical trials. Find 5 benefits here.
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.
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.
May is Mental Health Awareness Month, and Castor initiated a conversation about well-being at work and mental health in general. Read more: