Pharmaceutical R&D/Regulatory Professional
I Am Mahesh Pratapwar.
I am Pharma Professional, having skill of Pharmaceutical Product development and Complying with Regulatory Specifications for Pharmaceutical products according to guidelines of US/Europe/CDSCO.
I have completed M.Pharm (P.Ceutics).
Work experience more than 6 years in Pharma Industry.
Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing. ... Pharmaceutical companies use all the data accumulated during discovery and development stages in order to register the drug and thus market the drug.
Skills: Formulation & Development, Stability studies, QbD, OSD, Oral Liquids, Topical/Derma, DRA, CTD & eCTD, Plant exposure, Bioequivalence, DoE, etc...
Published more than 3 Research and review articles in high impact journals.
Top 9 pharma courses has been published on Udemy
1. Pharma Drug Regulatory Affairs Course - DRA 2022
2. Pharmaceutical Clinical Bioequivalence study (BA/BE) course
3. Clinical Research Certificate Course
4. Pharma eCTD & CTD preparartion + Sumbmission course
5. Complete Qbd: Quality by Design in Pharmaceutical Product Development
6. DOE-Design of Experiment in pharmaceutical development
7. Regulatory Affairs USFDA Electronic Submission Course
8. GMP Tablet Manufacturing Technology & Pharmaceutical Practices.
9. IPQC tests for Pharmaceutical Tablet dosage form
Other published courses:
Complete Website Design/Development Course (without code or programing language)