Brawn Laboratories Limited - Pharma Quality Product, Pharmaceutical Quality Product, Pharma Contract Manufacturers, Pharma in  India, Pharmaceutical Exporters, Indian Pharma Exporters, Pharmaceutical Exporters in India
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Quality
ISO 9001:2000, 13485, WHO : cGMP
BRAWN is proud to be awarded with the following certificates: ISO & WHO cGMP Certified Pharmaceutical Manufacturers.


 



Quality has always been a never-ending process at BRAWN, which has brought the international boundaries closer, with a world appearing smaller. Quality management has been a passion. Each unit that is manufactured is guaranteed with a promise of quality because of the total observation of the standard systems. Not only do the strictest quality standards apply to the products and raw materials, they are integral to all phases of plant operations, manufacturing, processing and procedures.

BRAWN is proud to be awarded with the following certificates: WHO cGMP Certified Pharmaceutical Manufacturers and ISO 9001:2000, 13485 Certified Pharmaceutical Manufacturers. Recently we also received the Schedule M Certification. We believe that clinical success is certain when the diagnostic skills of clinicians are complemented with the appropriate therapeutic regimen with precise standards of Quality.

Besides the well-established quality systems to ensure the product conformance requirement, the company has in-house specifications and standards for raw materials, packing materials and finished products. Quality manual is the first level document, which describes the quality system established and implemented in the organization according to quality policy, objectives and requirements of ISO 9001:2000, 13485 series and WHO cGMP.

We have in-house R & D and Quality Control Department (QCD) with the required laboratories. QCD is well equipped for analysis of Pharma APIs & Excipients. Testings are carried out by well-qualified, trained and experienced staff. All the machines and instruments are time to time checked for possible errors and calibrated regularly. Raw materials are inspected & tested for each consignment against relevant quality plan and released for production only after its approval by QCD. The in-process inspection activities are carried out regularly as per in-process Quality Plan. Finished product is inspected as per relevant Finished Product Quality Plan. Finished product is finally released after it passes all quality and approval tests.

 


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