Our Team. Our Facilities.
Our Processes.
cGMP Quality Assurance
The entire staff at GLP MED is intimately involved in our robust quality training program to ensure every team member is up-to-date on the latest requirements, as well to provide a constant reminder of the importance of quality. All departments from manufacturing and packaging personnel to the quality assurance line inspectors to upper management believe that quality is built-in. We instill this value in each team member to ensure they are performing their job to the highest level of quality, and as result our products are produced correctly.
SOPs are continually updated and employees retrained as we improve our processes. Internal non-conformances and outside complaints are thoroughly investigated by our quality operations team to determine root cause, implement CAPAs, and perform periodic effectiveness checks. Each step of the batch record from equipment set up to manufacturing, packaging, and testing is always double checked and then reviewed again by the designated quality assurance auditor. Regularly scheduled internal audits as well as outside agency and customer audits are routinely performed. Audit comments and findings are logged, reviewed, and used to promote continual improvement throughout the facility.
FDA Registered
cGMP Compliant
ISO13485:2016 Certified
Customer Quality Requirements
Not only do we follow FDA guidelines, but we also adhere to customer corporate quality requirements. We welcome quality assurance company auditors to our facility.