Parexel successfully completes CRO registration with CDSCO

Mumbai: Parexel, a clinical research organisation (CRO) providing the full range of Phase I to IV clinical development services, has announced the successful completion of its Clinical Research Organization (CRO) registration with the Central Drugs Standard Control Organization (CDSCO).

This registration complies with the new G.S.R 581 (E) regulation, which mandates all CROs operating in India to register with CDSCO.

Sanjay Vyas, President and Managing Director of Parexel India and Global Strategic Business Unit Head for Clinical Logistics & Global Safety Services, said, “This registration reflects our ongoing commitment to meeting regulatory requirements and upholding the highest standards in clinical research. This registration enables us to continue supporting our customers in bringing life-saving treatments to patients safely and efficiently.”

With over 40 years of global experience and a workforce of more than 6,000 in India, Parexel advances clinical research across complex therapeutic areas. 

Read also: CDSCO panel opines Paraxel to study either CKD or heart failure in phase IIb trial of AZD9977,Dapagliflozin FDC

Parexel provides the full range of Phase I to IV clinical development services. Parexel was the recipient of the 2024 and 2023 Society for Clinical Research Sites (SCRS) Eagle Award for advancing the clinical research profession through strong site partnerships, named “Best Contract Research Organization” in November 2023 by an independent panel for Citeline, and “Top CRO to Work With” by investigative sites worldwide in the 2023 WCG CenterWatch Global Site Relationship Benchmark Survey.

Read also: CDSCO panel opines Paraxel to study either CKD or heart failure in phase IIb trial of AZD9977,Dapagliflozin FDC

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