Good Manufacturing Practice (GMP) underpins the quality systems of US Food and Drug Administration (FDA) regulated products, including permanent and single-use medical devices. GMP medical device standards embrace an umbrella approach to regulation, as the sheer variety of devices available makes it impossible to establish individual GMP standards per product type, from diagnostic equipment and pharmaceutical delivery systems to permanent implants and prostheses.
Jordi Labs has decades of experience working within the regulatory framework for medical device development and manufacture, providing industry-tested and GMP compliant analytical services. We continuously ensure due-diligence is maintained throughout every process to meet and exceed the necessarily high standards established by GMP medical device
regulations.
Jordi Labs: GMP Medical Device Compliant Services
Jordi Labs chemists provide industry-tested solutions for quality assurance and control (QA/QC) processes in medical device manufacturing. With a wide range of FDA-compliant analytical solutions, you can rely on Jordi Labs to meet the stringent standards of GMP medical devices at every link in the production chain. Contact a member of the Jordi Labs team today if you have any queries.
