Shilpa Medicare arm Raichur API facility gets GMP Certification from ANVISA-Brazil

Written By :  Ruchika Sharma
Medically Reviewed By :  Dr. Kamal Kant Kohli
Published On 2024-07-10 06:01 GMT   |   Update On 2024-07-16 15:31 GMT
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Karnataka: Shilpa Medicare Limited's 100 percent subsidiary, Shilpa Pharma Lifesciences Limited's Active Pharmaceutical Ingredient (API) manufacturing facility, Unit II, situated at Raichur in Karnataka state has received GMP Certification from ANVISA-Brazil.

The GMP inspection was conducted at the facility from April 15-April 19, 2024.

The facility is involved in manufacturing various oncology and nononcology APIs.

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"The company remains committed to maintain the GMP status and quality standards as per the expectations and standards of Global Regulatory Authorities," the Company stated.

Read also: Shilpa Medicare CDMO customer reports positive results from Oxylanthanum Carbonate trial

Shilpa is an integrated pharmaceutical group, headquartered at Raichur, Karnataka, India, with business interests in niche Oncology & Non-oncology APIs, Peptides, Polymers, differentiated finished dosage formulations including orally dispersible films & transdermal patches along with biological portfolio. Shilpa also provides end-to-end CDMO services to global pharmaceutical companies across all its business segments based on its R&D and manufacturing capabilities backed by four R&D units and seven manufacturing facilities.

Read also: USFDA concludes inspection at Shilpa Medicare Hyderabad unit with zero observations

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