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Regulating Digital Therapeutic Cybersecurity: Today and Tomorrow
Cybersecurity has become a concern for Digital Therapeutics (DTx) developers and regulatory bodies. Learn to balance functionality &...
How to Incorporate Remote Technology in Your Next Medical Device Trial
Researchers are looking to incorporate remote technologies into medical device trials for a wide range of device classifications....
Digital Therapeutic Cybersecurity: Know Your Data Flow
A robust digital therapeutics cybersecurity system is integral to protecting users’ sensitive information helps meet regulatory requirements and...
How Decentralized Trials Can Support Meaningful Diversity
The Castor team is thrilled to see an increasing emphasis on diversity of race, gender, and even geography...
3 Ways eConsent Tackles the Challenges of Modern Clinical Trials
Although eConsent struggled to gain momentum and wider acceptance pre-pandemic, it's now a major part of clinical research....
Digital Therapeutic Cybersecurity: Keeping Participant Data Safe
DTx represent an emerging field of software-driven, evidence-based products intended to “prevent, manage, or treat a medical disease...
How Medical Device Trials Can Benefit from Decentralized Methods
At Castor, we hope to see DCT extend into all trials as we work alongside researchers in the...
The evolution of eConsent
Since it was first instituted in the 1960s, written consent to participate in research studies has undergone very...
8 Data Types to Collect Remotely
Decentralized clinical trials (DCT) are collecting many kinds of data remotely, and this data is only expected to...
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...
Developing an Infrastructure for Patient-Centric Decentralized Trials
Castor and Lightship discuss the infrastructure needs for providing the best patient experience and ensuring data integrity in...
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...
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...
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...
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...
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+...
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...
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...