Tejaswini Padole

About Tejaswini Padole

Hello there, Thanks for stopping by. I\'m currently working as DRA Officer at Ajanta Pharma, Kandivali Mumbai. In my role, I\'m responsible for drafting clinical as well as non-clinical regulatory documents such as Periodic Safety Update Report (PSUR), Risk Management Plan (RMP), Periodic Benefit-Risk Evaluation Report (PBRER), Query Action Plan (QAP) etc. In my previous role as Junior Regulatory Affairs Specialist at LabCorp Drug Development, Pune, I contributed for creating and updating product specifications in accordance with Product Data Health (PDH) and Data Quality Index (DQI) guidelines. I\'ve a genuine interest and passion for Regulatory Affairs Industry. I\'ve completed my Masters in Pharmaceutics Department of MET\'s Bhujbal Knowledge City, Adgaon Nashik. I also hold PG Diploma in Drug Regulatory Affairs (DRA) from NDMVP College of Pharmacy which is a MSBTE Approved Program. I\'m always excited to learn from people in the different sectors and evolve as an individual. Looking forward to you for your knowledge and expertise.

Experience

1. Officer Dra Clinical

   Ajanta Pharma Ltd

   Jan 2024 — Present · Mumbai, IN

   In this job-role, I\'m responsible for documentation of clinical as well as non-clinical modules. These modules includes; Periodic Safety Update Report (PSUR) Risk Management Plan (RMP) Periodic Benefit-risk Evaluation Report (PBRER)Quality Action Plan (QAP)

Education

• MET's IOP Bhujbal Knowledge City, Metleague Colleges, Adgaon, Nashik

  M. Pharmacy

  2021

• School of Pharmacy, S.R.T.M.U.Nanded

  Bachelor of Pharmacy - BPharm

  2016 — 2020