Pharmacovigilance and Regulatory Affairs

The Pharmacovigilance and Regulatory Affairs team at Polpharma is responsible for ensuring the safety and efficacy of the company's pharmaceutical products throughout their lifecycle. This team monitors adverse effects, compiles and analyzes safety data, and ensures compliance with global regulatory standards. By working closely with clinical trial specialists and regulatory strategists, they play a vital role in guiding the company's decisions on drug development and market authorization.