Regulatory Affairs

Regulatory affairs for clinical trials is the major part in the clinical trials approaches. Every clinical trial must be conduct according to the Regulatory affairs guidelines. There are several Regulatory affairs depending upon the countries. Regulatory Affairs departments are growing within companies. Global harmonization in standards has led to consistent approach in regulatory submissions and hence its review.

  • Regulatory Guidelines
  • USFDA
  • EU
  • MHRA

Related Conference of Regulatory Affairs

Regulatory Affairs Conference Speakers