About us

SIPRA Labs is a Govt. approved and ISO-9001:2000 Certified state-of-the-art Pharmaceutical / Analytical laboratory set up for providing specialised services for

 Bio-Availability
 
• Bio-Equivalence
 • Stability and method development studies

The other major thrust areas of SIPRA Labs are Research and Development of Pharmaceuticals and Drug Intermediates.

Impurity profile estimation, Study of Drug release patterns and Environmental Impact Assessment studies.

In order to meet all the above requirements of our clients, SIPRA Labs set up its facilities at Hyderabad, the nerve center for Indian Drug Industry, with a capital outlay of Rs. 25 million. It is well equipped with state-of-the-art electronic instruments and an experienced team of young and enthusiastic scientists for providing professional services in the field of Drugs, Pharmaceuticals, Chemicals, Foods, Process wastes and environmental studies.
 

Sipra Labs adheres to the following quality standards:

• Indian Pharmacopoeia - IP
• US Pharmacopoeia - USP
• British Pharmacopoeia - BP
• European Pharmacopoeia - EP
• Japanese Pharmacopoeia - JP
• Association of American Chemists - AOAC
• Bureau of Indian Standards - BIS
• ISO 9002 Standards (Australia, Quality Assurance Services)
• Drug Control Administration (Government of India)
• Good Laboratory Practices Recognized Research Institution,
• Andhra University - Waltair
• DST Accreditation

 

Awards:
We received several awards from the chemical and pharmaceutical industry in recognition of high quality service.

• ISO 9002 certification from Bureau Veritas Quality International.
• The Drug Controller General (India) approval for conducting Bio-Availability & Bio-
   Equivalence studies for new drugs.
• Approved by Drug Control Administration Govt. of Andhra Pradesh & India. as a
  testing laboratory.
• Procedures for getting the approval from Andhra Pradesh Pollution
  Control Board, Hyderabad
• Recognised as a research center by some Indian Universities

 

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