Profile Summary
Dr. GURDEEP SINGH S.
I have hands on R & D exposure of 42+ years in the development of new synthetic methodologies for carbocyclic...and heterocyclic compounds, natural product as well as Organometallic Chemistry. ( 13 international publications...
Dr. Kelvin C.
As a highly skilled professional with a PhD in Mathematics, an MSc in Computer Science, and a BSc in Engineering, I have a broad range of exper...
Dr. Ahram Q.
My professional background is to technically write the Scientific content, assess the researcher in research work related to Bioinformatics and...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
I am managing R & D project for in-vitro diagnostics, in-vitro drug screening, medical device, and vaccine development. I look into all as...
Dr. Stuart C.
Pharmaceutical/Nutraceutical/Food Formulation Scientist with 30+ years of experience developing soft chews, tablet and capsule products, chewab...
Dr. Precious O.
I am experienced in
Dr. Dr. Kritee P.
I am a scientist with more than 9 years of experience in the field of chemistry for healthcare applications esp. on cancer research using molec...
I lead and support drug development and production for clinical development and commercial products. I have two years working experience in pha...
Dr. Harsh V.
A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...
Dr. Bharat K.
Quality by design: Build quality into drug product from early development Extended release: Formulation of tablets, capsules, and suspensions f...
Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...
Pharmaceutical Regulatory Affairs professional with more than 10+ years in industry experience in Formulations.
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 ...
SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...
Vandita S.
Expertise in Development of innovative, green & cost effective products & processes for Nutraceuticals, Dietary supplements, Cosmetic...
Lakshmi Deepthi S.
15 years of experience in Biopharmaceutical/Biosimilar industry with end to end understanding of product development, CMC regulatory strategy a...
Sada Siva R.
Biosimilars Regulatory submission for developed markets , LCM , dossier preparation and Stratagy. SME for Analytical development and Biosimila...
I have following experiences: >Research work like Articles >Basic networking concepts >Teaching Skills >Android...
Christine F.
Lab-trained writer known for reliability and versatility. Effective collaborator. Skilled in technical writing and data analysis. Background in...
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