Ramesh M.

Ramesh M. is a Regulatory Affairs Specialist at Sahajanand Medical Technologies since February 2017, with expertise in managing technical files, compliance with CDSCO, India MDR, EUMDR 2017/745, and ISO standards. Previous experience includes roles as Business Consulting Manager for Regulatory Services at MakroCare, Senior Research Associate at Aragen Life Sciences, and Senior Research Analyst in Clinical QC/QA at QPS Bioserve. Ramesh began the career as an Executive at Dr. Reddy's Laboratories. Ramesh holds a postgraduate degree in Pharmaceutical (Formulations) Sciences and a bachelor's degree in Pharmaceutical Sciences, with education extending from general studies to specialized sciences.