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.
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