We follow several strict in-house Quality Assurance and Quality Control (QA/QC) procedures to ensure that all of our products are completely sterile and safe before distribution to the client. These processes are overseen by our full-time QA/QC manager, who works closely with FDA consultants to ensure that we not only comply with all FDA regulations, but that we exceed these requirements. Our QA/QC testing includes:
After sterile manufacturing is complete, the quality of our products is confirmed using the latest innovative technology. These tests are all performed in-house for further quality assurance with our state-of-the-art equipment.
As a 503B FDA-registered outsourcing facility, we comply with all FDA regulations and cGMPs.
"Axia Pharmaceutical‘s core values — patient safety, flawless quality, operational excellence, top-notch customer service, and a respectful and collaborative work environment —best define our organization and our people. They also form the nucleus of what differentiates Axia Pharmaceutical from others in our industry."
- Chief Executive Officer