About Sipra

| About Us


SIPRA LABS LIMITED is a global Contract Research Organization (CRO) offering Regulatory Compliant Research and Developmental Services to Pharma, Biotech and Medical Device Companies since two decades.  Sipra  is USFDA registered & DSIR approved R & D center.

Sipra Labs Limited was established in 1994, with an objective to provide quality testing services to the leading Generic, Pharma, biotech and Medical device companies and now it has become renowned contract research organization not only in India and also across the globe. Its immense experience, expertise and infrastructure have carved Sipra as a preferred destination for the all research needs of its esteemed clientele, which includes many domestic & global companies. It is a contract research organization with independent infrastructure and fully engaged in providing Analytical, Microbiological, Stability testing, Method development & Validations, Clinical, Pre-clinical, Bio-equivalence/ Bio-availability, Food & Safety and Medical device testing services. It has a team of dedicated scientists working on various research projects outsourced by renowned organizations for their submissions to various regulatory bodies.

It has been approved by USFDA, TGA (Australia), Health Canada (Canada) and also accredited with National accreditation board for testing and calibration laboratories (NABL) as per ISO/IEC 17025 (Chemical, Biological, Mechanical and Radiological testing), ISO 15189:2007 (Medical Testing), Drug controller of administration (DCA), Drug controller general of India (DCGI), Bureau of Indian standards (BIS) and Good laboratory Practice (GLP). The facility is cGMP certified and performing the quality activities in line with OECD principles of Good laboratory practices.


  • BA BE studies
  • Pre-Clinical Studies 
  • Genotoxity Studies
  • In-Vitro Biological Studies
  • Method Validation
  • Drug characterization
  • Stability Studies
  • Molecular Weight Determinations
  • Pharmacokinetic Studies
  • Pre-Clinical Studies
  • DNA Reacting Impurities
  • Impurity Profile
  • Extractables & Leachables


To be a leading one stop service provider globally for drug development services with a wide ranging regulatory compliance and acceptance.To offer benchmark services with superior competitiveness by continuously upgrading the infrastructure and the quality of research for betterment of human life.


We are committed to satisfy our customers by providing products and services that consistently exceed the expectations in terms of quality, delivery and competitiveness. Committed to offer need based excellent pre & post support services to our customers in meeting their regulatory & research requirements. Committed to work with unfailing social and environmen