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.