At Signant Health, we combine our technology with robust clinical, scientific, and regulatory expertise to guide your study from design to regulatory submission. In this video series, Chief Medical Officer Dawie Wessels leads discussions with a selection of our in-house clinicians, scientists, medical practitioners, and key opinion leaders about how they ensure the best practices and solutions are in place to help clinical research programs succeed.

Want to Learn More?

Optimizing Pediatric Trials to Generate High Quality Data for Regulatory Decision-Making   

Patient Selection and Monitoring Ratings Validity in Mood Disorder Trials   

Optimizing Oncology Trials to Generate High-Quality Data for Regulatory Decision-Making 

Seeking Signal Detection in Schizophrenia Trials: Lessons Learned   

Important Considerations for the Successful Migration of eCOA  

Optimal eCOA for 
Vaccine Trials   

Baseline Score Inflation: 
Detection, Impact, and Mitigation

The Double-Blind Placebo Run In: To Be or Not to Be?   

Novel Endpoints in Parkinson's Disease Trials

Leveraging DCT in Dementia Studies

What makes a successful rater training program?