SIPRA LABS is USFDA registered and DSIR approved Contract Research Organization engaged in Drug Development support services to the Pharma Industry. The Centre has a team of 150 scientists engaged in different innovative Research Projects for global regulatory submissions. The thrust of the Organization is to create one-stop-research solutions to the Drug and Pharmaceuticals Industry. SIPRA, a dedicated research organization, collaborates with the industry in conducting the studies as per GLP / GCP guidelines. SIPRA is preferred research organization for the clients across the globe.
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Specialization
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- Crystallography studies
- Genotoxicity
- Impurity profile
- Metabolic studies
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- Novel Drug Delivery System
- Method Validation
- Stability Studies
- Cytotoxicity
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Accreditation
- USFDA registered cGMP control testing laboratory
- Department of Science & Industrial Research approved R & D Centre
- Drugs Controller General of India (DCGI) approved BA/BE center
- Department of Biotechnology approved Institutional Bio-Safety Committee (IBSC) for RCGM products
- NABL accreditation for Chemical and Biological as per ISO - 17025, Medical Testing as per 15189
- ISO-9001:2000 Quality Management Systems
- Drugs Control Administration (A.P)
- Recognized by Bureau of Indian Standards
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