Understanding the EU Clinical Trials Regulations Updates
The new European Union regulations have significant implications for sponsors submitting trials in the EU.
Advarra® Regulatory Consulting
If you’re looking for help in the development of innovative life science and digital health products, then Advarra is the answer.
Pitfalls of Chemistry, Manufacturing, and Controls in Investigational New Drug Preparation
Submitting an Investigational New Drug (IND) application for the first time? Consider three common CMC pitfalls that may impact submission.