Profile Summary
Kishor U.
I have a Master's degree in pharmacology with about 7 years of experience in both CMC and the Clinical domains of regulatory affairs. I am ...
Suresh S.
Pharmaceutical Regulatory Affairs professional with more than 10+ years in industry experience in Formulations.
Rachid E.
My qualification is an MSc in Biomedical Sciences. I am a Regulatory Affairs Specialist. The primary responsibilities are: - Working with CTD ...
Surya N.
SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...
Lakshmi Deepthi S.
15 years of experience in Biopharmaceutical/Biosimilar industry with end to end understanding of product development, CMC regulatory strategy a...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Ash P.
Highly motivated and scientifically driven regulatory professional with over 15 years of experience in the biopharmaceutical industry, spanning...
Christine F.
Lab-trained writer known for reliability and versatility. Effective collaborator. Skilled in technical writing and data analysis. Background in...
Rao M.
Biosimilars Regulatory submission for developed markets , LCM , dossier preparation and Stratagy. SME for Analytical development and Biosimila...
Majid A.
I have following experiences: >Research work like Articles >Basic networking concepts >Teaching Skills >Android...
Anand K.
Regulatory Affairs Services like ANDA, ANDS, Pre-IND, Control Correspondence, DMF, APIMF, CEP, and Dossier (Rest of World).
Dana D.
Award-winning author and technical writer with expertise in content strategy, copywriting, and SEO-optimized storytelling. Experienced in craft...
Dr. Muhammad Akbar R.
Dedicated Public Health Researcher and Healthcare Professional with extensive experience in epidemiology, maternal and child health, and optome...
Dr. Raj V.
Experienced scientific and regulatory affairs professional, trained in drug discovery and development working with novel small molecule drugs, ...
Majid T.
I have several years of experience as a scientific editor and peer reviewer for a wide range of high-impact journals and international conferen...
Shaheen Fathima A.
I am a Regulatory Affairs and Clinical Research professional with expertise spanning drug development, compliance strategy, and scientific docu...
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Likhit M.
I am a pharmaceutical scientist with 13+ years of experience in analytical R&D, regulatory documentation, and complex generics—including op...
Roselyn B.
With a profound years of experience in the food industry, I specialize in turning innovative concepts into compliant, market-ready products. I ...
Dr. PRIYANKA M.
I am a PhD-trained biotechnology professional and experienced scientific writer with a strong foundation in molecular biology, human genetics, ...
Deepak D.
Highly motivated Regulatory Affairs professional with strong expertise in U.S. FDA 510(k) submissions, Indian import licensing (CDSCO), ISO 134...
Dr. Kira G.
PhD in chemistry, trained across organic synthesis, pharmaceutics, in vitro diagnostics and drug delivery
Sohanur R.
Pharmaceutical quality and compliance specialist with over 15 years of experience in sterile manufacturing environments. Holds a Master’s degre...
Henvi P.
I am a Bachelor of Pharmacy graduate and a QA Executive at a medical device company specializing in orthopedic products. With hands-on experien...
Dr. Robin A.
I deliver audit-grade, regulator-defensible, visually flawless governance and scientific documents that survive FDA, EMA, and courtroom scrutin...
Dr. Mia W.
I am a formulation scientist with experience in pharmaceutical R&D and preclinical nanomedicine research, including developing drug deliver...
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