PharmaCore® has developed an outstanding state-of-the-art facility to serve the growing need for GMP clinical material and bulk active pharmaceutical ingredients (APIs) accompanying the rapid pace of drug discovery.

The PharmaCore® GMP manufacturing facility includes:

• Two validated GMP clean room synthesis laboratories to ensure the quality of manufacture of multi-kilogram quantities
• Large capacity glass reactors
• Large-scale vacuum evaporator equipment in walk-in hoods
• Sophisticated organic chemistry laboratories
• Advanced analytical capabilities in HPLC, NMR and LC/MS

PharmaCore®’s specially trained, GMP manufacturing team operates under the USFDA Guidelines for Bulk Pharmaceutical Chemicals (BPC), www.fda.gov, and is backed by a comprehensive documentation system.

Customers are invited to discuss GMP projects and audit the PharmaCore® facilities.