Operating state-of-the-art automated sterile injectable lines, oral solid dosage (tablets/capsules) manufacturing, and dedicated antibiotic blocks conforming strictly to WHO-GMP and international pharmacopoeial standards (USP/BP/IP).
Directed by Veteran Formulation Pharmacists (M.Pharm, Ph.D.) and Regulatory Affairs Specialists with over 32 years of global pharmaceutical manufacturing excellence.
1. Submit formulation requirement & batch MOQ. 2. Review COA/CTD dossier stability data. 3. Pilot batch validation, bulk run & cold-chain dispatch.
Comprehensive Pharmacovigilance tracking and active Cold Chain (2°C - 8°C) monitoring guarantee complete product efficacy from plant to patient.