Regulatory Affairs and Quality Management

The Regulatory Affairs and Quality Management team at Cipla plays a critical role in ensuring that all pharmaceutical products comply with local and international regulatory standards. This team is responsible for managing submissions to regulatory agencies, overseeing quality assurance protocols, and ensuring compliance with Good Manufacturing Practices (GMP). By collaborating closely with various departments, they strive to facilitate product approvals and maintain the highest standards of quality across Cipla's diverse therapeutic offerings.