GLP Auditor 2

Profile: A Pharma professional with more than 20 years of experience in Clinical Development (Bioequivalence Studies, Clinical Trials, Nutraceutical/Cosmetic efficacy studies), Project Management for Formulation Development and Clinical Research. Domain and Training expert for topics on Clinical Development, QMS/GDP and GCLP/GLP. *Experience in Setting-Up and Building International Technical competence centers. Proficiencies are Clinical Development /Operations & QMS, CRO Management/PK/PD end point study Management, Clinical Development [Generics, 505 (b)(2)], Auditor for GCLP, QMS and Data Integrity, Alliance & Business Development – Finished Dosage. With Regulated Warehouses Spread across Canada, US, Brazil, UK & offices across Germany, USA, and Singapore, we can help our partner with unmatched reach and Best Quality in Services. Based in Hyderabad.