Preclinical research in India
India’s preclinical CRO sector is centered on Bengaluru, Hyderabad, Pune and Ahmedabad, offering discovery biology, chemistry, DMPK and GLP toxicology to international sponsors, often at lower cost than US or European labs.
India is a full adherent to the OECD Mutual Acceptance of Data system, with GLP compliance monitored by its National GLP Compliance Monitoring Authority, so GLP studies from certified Indian facilities are accepted by member regulators. Animal experimentation is overseen by the national committee CCSEA.
Preclinical CROs in India
Showing 1 CRO with a site in India. Order rotates daily so no lab is permanently listed first.
Questions to ask a CRO in India
- Will the study run at the site in India, or could work be moved to another of your facilities?
- How do you receive test article shipments, and what import permits or customs paperwork do you handle?
- Can our team visit the facility before the study starts and during critical phases?
- Which regulators and GLP monitoring authorities have inspected this site, and when?
- What is your current lead time for our species at this site?
For a full checklist, see our CRO selection guide.