MENADIONA is a well established European API manufacturer with extensive experience in Regulatory affairs, GMP compliance, ISO 9001 certificate, and inspected by most Health Agencies worldwide. CONTRACT MANUFACTURING is a key activity at MENADIONA. We produce Intermediates of very different features for third parties, under exclusivity and NDA, with long term partnership.

Type of Drugs Manufactured:

Small Molecule

CDMO Services:

Drug Substance Manufacturing (API)

No. of Manufacturing Facilities:

2

High Potent Products capabilities:

OEB 3

Facilities Locations:

Europe

Regulatory Approvals for facilities:

FDA (United States);ISO;GMP;PMDA (Japan)