Our Certification consists of 4 modules: Pharmacovigilance, Clinical Research, Clinical Data Management & Regulatory Affairs.
These modules will help new graduates to have the complete understanding of Drug Development, right from Preclinical to Post Marketing Surveillance.
It also gives insights about the Regulatory approvals, product registration across various regulatory authorities, etc.
Our Pharmacovigilance module will help understand the latest PV processes, right from collection, detection, assessment, monitoring, & prevention of adverse events for various drugs or cosmetic products.
- The course is designed keeping a fresh graduate under consideration.
Career Option with this course:
- Pharmacovigilance Associate
- Regulatory Affairs Associate/Executive
- Clinical Research Associates/Coordinator
- Principal Investigator, Sub-Investigator
- Submission Specialist
- Clinical Data Associate
- Medical Reviewer
- Audit Executive
- Quality Control, Quality Analyst
- Medical Coder
All these profiles start with Junior Associate and go up to Director/VP in any organization.