About Us - Facilities

The Azopharma Product Development Group operates 12 research facilities and two manufacturing facilities. We operate within current Good Manufacturing Practices, Good Laboratory Practices and Good Clinical Practices, and we have an independent Quality Assurance department for our operations. Quality Assurance ensures all data is 100% reviewed and every report is checked in duplicate. Our facilities are FDA and USDA registered and inspected, licensed to handle DEA controlled substances and client audited on a routine basis.

We employ scientists with unique combinations of education, experience and training pursuant to guidelines dictated by the Code of Federal Regulations (CFR). Instrumentation and equipment utilized in our facilities have operational, performance and calibration criteria and records to ensure complete data traceability. This combination of business, compliance and training systems offers our clients a compelling solution in product development.

Our facilities are located throughout the world with offices in Florida, New Jersey, Missouri, California and Europe. For more information about our individual facilities please visit our affiliate websites:

Azopharma Contract Pharmaceutical Services
Cyanta Analytical Laboratories
AniClin Preclinical Services
IQsynthesis
AvivoClin Clinical Services
ApiCross Drug Delivery Technologies
ADMEQuant