
CuraTeQ Biologics Private Limited, a wholly owned subsidiary of Aurobindo Pharma Limited, has secured GMP approval from ANVISA, Brazil's National Health Surveillance Agency, as per the exchange filings.
The approval covers the company's biosimilars manufacturing facility in Hyderabad, strengthening its regulatory footprint in international markets.
The Hyderabad facility underwent a GMP inspection conducted by ANVISA between May 11 and May 15, 2026.
Approval was granted following the successful inspection of the facility for biological API and sterile products manufacturing.
The inspection assessed 4 biosimilar products along with the mammalian and microbial drug substance manufacturing facilities.
It also covered the prefillable syringe and vial filling facilities, packaging and labelling operations, as well as quality control testing and product release laboratories.
CuraTeQ's drug substance and drug product GMP facility already holds certifications from the European Medicines Agency (EMA) and the World Health Organization (WHO).
According to the company, the ANVISA approval reaffirms its commitment to global quality standards and regulatory compliance while strengthening its ability to supply biosimilar products across Brazil and the broader Latin American market.
As of 22 July 2026, at 11:00 AM, Aurobindo Pharma Limited share price was trading at ₹1,525.90 per share, reflecting a decline of 3.41% from the previous trading session.
The ANVISA approval marks another regulatory milestone for CuraTeQ Biologics, enhancing the global recognition of its Hyderabad manufacturing facility and supporting the company's expansion in the Brazilian and wider Latin American biosimilars market.
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Published on: Jul 22, 2026, 12:21 PM IST

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