Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies.
With over 30 years of GLP compliance and certification, Eurofins Advinus serves diverse industries such as Biotech, Pharmaceutical, Biological, Agrochemical, Nutraceutical and Cosmetic. Eurofins Advinus is the only contract research organization (CRO) in India to have developed data in support of 90+ end-to-end IND enabling packages to be submitted to global regulators such as USFDA, EMA, MHRA, Health Canada and others.
Analytical method development and validation
Extraction method optimization in complex matrices (soil, sediment, plant parts, animal tissues, etc.)
Handling and troubleshooting HPLC, GC, LCMS/MS, and GC-MS/MS
Metabolite identification and reporting
MSc in Analytical Chemistry / Organic Chemistry / General Chemistry
Experience & Expertise:
10+ years of industry experience
Minimum 6 years as a Study Director in a GLP-compliant facility