Keeping you in the Loop
There is an evolving landscape for the development and regulatory compliance of therapeutics and medical devices.
Here we try to keep you informed on relevant articles, news and our expertise to help your business.
Environmental Risk Assessment For Drug Submission
An essential part of the regulatory submission - important to consider early
QPs – Critical Regulatory Role for Biopharma Manufacturing
Peritus Regulatory have experienced QPs to support your business needs.
Don't Forget CMC in Drug Development
What’s this CMC and Why should I think about it early in development?
