Cyanta offers QC and microbiological testing for Active Pharmaceutical Ingredients (APIs), pharmaceutical intermediates, excipients and finished products.

Cyanta has hundreds of standard operating procedures, rigorous compliance systems and a detailed training program that allows for successful execution of quality control testing. Our QC analytical laboratories ensure that your products are safe and efficacious from the raw material to the finished product.

Methods utilized for QC services include

• Client methods
• In-house developed and validated procedures
• USP methods
• PhEur methods
• JP/JPE methods
• BP methods
• ACS monographs
• AOAC testing
• DAB compendial tests
• FCC testing procedures

Cyanta supports the following pharmaceutical development activities in our QC services group:

• Non-traditional methods execution
• Testing of APIs and intermediates
• In-process testing support
• Process validation design and validation testing
• Finished product release and stability
• Container-closure testing