SIPRA, with two decades of experience, is the preferred destination for the research needs of its esteemed clientele, include many transnational companies.

SIPRA LABS is USFDA inspected, DSIR approved Contract Research Organization engaged in Drug Development support services to the Pharma Industry.

The thrust of the Organization is to offer one-stop-research solutions to the Drugs, Pharmaceuticals and Biotech Industry.

committed organization collaborating with industry in conducting research studies as per cGLP / cGCP guidelines.

Sipra Expertise, infrastructure and credibility are widely recognized across the globe and its services from characterization to dossier preparation, including pre-clinical studies, product development studies and clinical studies for pharma and bio pharma products.


  Crystallography studies
  Genotoxicity
  Impurity profile
  Metabolic studies

  Novel Drug Delivery System
  Method Validation
  Stability Studies
  Cytotoxicity