StockWatch
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Pharmaceuticals
Regulatory21 Jul 2026, 04:40 pm

Aurobindo Pharma Subsidiary's Biosimilar Facility Gets ANVISA Approval

AI Summary

CuraTeQ Biologics Private Limited, a wholly owned subsidiary of Aurobindo Pharma Limited, has received approval from Brazil's ANVISA for its biosimilar manufacturing facility in Hyderabad. The facility successfully passed a GMP inspection by ANVISA, covering biological API and sterile products, including four biosimilar products and various manufacturing and testing areas. This approval, following existing EMA and WHO certifications, enhances CuraTeQ's ability to supply biosimilar products to Brazil and the wider Latin American market, underscoring the company's commitment to global quality standards.

Key Highlights

  • Aurobindo Pharma subsidiary CuraTeQ receives ANVISA approval for biosimilar facility.
  • Facility passed GMP inspection for biological API and sterile products.
  • Approval strengthens supply to Brazilian and Latin American markets.
  • Reaffirms commitment to global regulatory compliance and quality standards.