Dr Ahammed Kabeer

Background

About Dr Ahammed Kabeer

Regulatory Affairs Executive with a solid foundation in pharmaceutical sciences and a Doctor of Pharmacy (Pharm D) degree I bring a comprehensive understanding of the regulatory environment surrounding medical devices. I have a strong knowledge of Indian Medical Device Rules (MDR) 2017 ensuring compliance with both national and international standards. My expertise includes preparing Drug Master Files (DMF) and Product Master Files (PMF) registering products preparing Clinical Evaluation Reports (CER) and addressing regulatory queries—all aimed at delivering safe and effective healthcare solutions to the market. In my current role I oversee the submission of regulatory filings and maintain active communication with health authorities to ensure regulatory compliance throughout the product lifecycle. I collaborate closely with cross-functional teams to align regulatory strategies with business objectives contributing to the seamless integration of compliance and innovation.