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
Recommended Sessions
- Case Report in Clinical Trials
- Pharmacokinetics and Pharmacodynamics
- PV Consultings And Bussiness Opportunity
- Adverse Drug Reactions
- Â PV Data Base Managemaent
- Case Study
- Clinical Data Management
- Drug Safety
- Entrepreneurs Investment Meet
- Good Pharmacovigilance Practice
- Growth Strategies in Pharma
- Overview of Clinical Trials and Post Marketing
- Pharmacovigilance on Biopharmaceutics
- Pharmacovigilance Risk management plans and new risk- benefit analysis tools
- Pharmacy Practices and its Challenges
- Preclinical and Clinical Trials on Various Disorders
- Regulatory Affairs