Preclinical CRO
Adita Biosys is an established Preclinical Contract Research Organization (CRO). We provide Preclinical Toxicity testing services in compliance with OECD GLP, Schedule L1 GLP and ISO 17025 standards. Adita Biosys support Medical Device, Agrochemical, Industrial Chemical, herbal, pharmaceutical and nutraceutical companies.
As an independent preclinical Contract Research Organization (CRO), we specialize in providing integrated preclinical studies and regulatory services that strictly adhere to Good Laboratory Practice (GLP) principles. Our team conducts biocompatibility and preclinical research in line with national and international guidelines, including but not limited to ISO 10993, ASTM, OECD, ICH, FDA, NDCT, CIB & RC. Adita Biosys ensures high-quality services, swift turnaround time, and cost-effective services.
Accreditations and Approvals
- OECD Good Laboratory Practice (OECD GLP): From national GLP compliance Monitoring Authority.
- CIB & RC: Approved by Central Insecticides Board & Registration Committee Government of India
- DTL: Approved by State drug controller as a government approved drug testing laboratory for carrying out tests on drugs / cosmetics, and raw materials used in manufacture on behalf of licensees for manufacture and for sale of drugs / cosmetics
- Good Laboratory Practices (GLP): As stipulated under "Schedule L-1" of the Drugs and Cosmetics Rules.
- ISO 17025 Accreditation: From NABL (National Accreditation Board for Testing and Calibration Laboratories)
- ISO 9001:2015 Accreditation: From AQC Global LLC
- CCSEA Registered: Department of Animal Husbandry and Dairying, Ministry of Fisheries, Animal Husbandry and Dairying, New Delhi
