Passionate Regulatory Affairs professional with over 9 years of experience of handling regulations of Medical Devices, Drugs, Biologicals and Alternative Medicines. Expert at the development and implementation of Quality Management System in compliance with Good Distribution Practices for Medical Devices (GDPMD) and Pharmaceutical guidelines. Having Pharmacovigilance reporting training. Provides technical support to the sales, marketing and other associated departments. Successful history of handling projects like obtaining licence to import medical devices and quality certification for company. Nominated as Industry (Secondary) representative of Asian Harmonization Working Party by DRAP.