I am a Doctorate in Pharmaceutical Sciences with 11+ years of experience, published 60+ research and review papers in various National and International journals also authored 3 Text Books and 1 Book Chapter. Nominated Advisory Member, Editorial Team Member and as Scientific Reviewer to 60+ National and International Pharmaceutical, Medical and Science journals.

People Management and Project Management (HCL Technologies, Tex Academy certified). Expertise in journal paper publications, scientific writing, using of online systematic review databases like PubMed, ScienceDirect, ScopeMed and EndNote tool.

Expertise in EU Regulatory requirements pertaining to Clinical Evaluation: MDR 2017/745; MEDDEV 2.7/1 revision 4. Expertise in Indian Medical Device Rules 2017-GSR78(E) dated-31.01.2017, Notified Medical Devices Regulations as per Drugs and Cosmetics Act 1940 and Rules made thereunder in 1945.

Expertise in Authoring and Reviewing Clinical Evaluation Plan, Clinical Evaluation Reports, Post Market Surveillance Plan, Post Market Surveillance Report, Post Market Clinical Follow-Up Plan, PMCF evaluation Report, Periodic Safety Update Report, Clinical Risk-Benefit Analysis Reports, Summary of Safety and Clinical Performance related to Medical Devices.

Knowledge on clinical trials and regulatory requirements. Expertise in Pharmacological screening methods and animal handling techniques, Natural products isolation and elucidation techniques.