Quality Assurance and Regulatory Affairs

The Quality Assurance and Regulatory Affairs team at Cipla ensures that all products meet stringent quality standards and comply with regulatory requirements across various geographical markets. This team oversees the development and implementation of quality systems and processes, provides guidance on regulatory submissions, and ensures compliance with Good Manufacturing Practices (GMP) for pharmaceuticals and medical devices. Their role is crucial in maintaining product integrity and safety, thereby facilitating Cipla's mission to provide accessible healthcare solutions globally.