Profile Summary
Surya N.
SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...see more
Reema D.
• Preparation of CTD sections of the dossiers required for Regulatory submission in various countries namely EU (National, MRP and DCP), US (AN...see more
Lakshmi Deepthi S.
15 years of experience in Biopharmaceutical/Biosimilar industry with end to end understanding of product development, CMC regulatory strategy a...see more
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...see more
Christine F.
Lab-trained writer known for reliability and versatility. Effective collaborator. Skilled in technical writing and data analysis. Background in...see more
Rao M.
Biosimilars Regulatory submission for developed markets , LCM , dossier preparation and Stratagy. SME for Analytical development and Biosimila...see more
Dana D.
Award-winning author and technical writer with expertise in content strategy, copywriting, and SEO-optimized storytelling. Experienced in craft...see more
Anand K.
Regulatory Affairs Services like ANDA, ANDS, Pre-IND, Control Correspondence, DMF, APIMF, CEP, and Dossier (Rest of World)....see more
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