The Pharmax facility is designed based on latest WHO GMP guidelines, meeting stringent quality standards. The built up area is approximately 100,000 sq feet.
The warehouse is designed for dedicated sampling of actives, in-actives and primary packaging materials. Approved and rejected materials are provided for staging of raw materials, packaging materials and finished products, there are also segregated areas for quarantine. The storage areas are under real-time temperature and RH surveillance.
The production block is designed to cater to demands of solid orald osage forms made through various granulation processes such as dry granulation, wet granulation and pallet coating (Wurster). All the stages of manufacturing and packaging are performed on automated lines equipped with precise and latest machinery meeting 21 CFR part 11 compliance from Bosch and CAM. The compression capabilities include IR, MR, DR and bilayer tablets. The capsule filling machine is capable of producing capsules filled with powders, pallets, mini-tablets and their combinations. Packaging capabilities include blister with multiple packaging combinations and bulk product packs.
The Quality Control department includes dedicated wet chemistry, instrumentation and microbiology laboratories. The laboratories are equipped with 21 CFR part 11 compliant advanced analytical instruments such as HPLC, GC, IR, ICP and other instruments for performing routine analysis. Stability chambers meet the stability conditions as per ICH guidelines.