Auro Laboratories has received World Health Organization-Good Manufacturing Practices (WHO - GMP) certificate from the Food & Drug Administration, Maharashtra, for its Active Pharmaceutical Ingredients (API) (Bulk Drugs) manufacturing located in MIDC Tarapur, Maharashtra. The certificate is valid up to September 30, 2028.
The company has received this certificate after it successfully completed WHO inspection at its API Tarapur manufacturing facility.
Auro Laboratories is a manufacturer of Active Pharmaceutical Ingredients (APIs), Intermediates and Generic Formulations.