Good Manufacturing Practice (GMP) is an essential system for guaranteeing that pharmaceutical goods are produced according to a stringent set of internal quality standards. It concerns individuals at every stage of the drug development chain, from the chemists designing and implementing clinical studies to the employees handling dosage form products at the end of the production line.
Jordi Labs provides a suite of pharmaceutical analysis solutions in accordance with current GMP standards. Whether screening incoming raw materials or performing good—bad comparisons of dosage form products, Jordi Labs guarantees a level of quality that meets the requirements of GMP pharma regulations. We can help you mitigate the commercial and ethical risks common to the manufacturing of pharmaceuticals.
Although GMP pharmaceutical standards are established by the US Food and Drug Administration (FDA), they are not merely a regulatory necessity. GMP represents a framework for enhanced quality assurance and control in the pharmaceutical market. With unmatched expertise in analytical testing and a practical understanding of the obstacles for new drug products in today’s market, Jordi Labs is committed to a robust set of GMP pharma standards that ultimately raise the bar for QA/QC.
GMP Pharma Testing with Jordi Labs
Jordi Labs was founded on the core beliefs of integrity and innovation, and our GMP pharma testing service embodies these values. With a broad range of FDA-compliant testing solutions, we can add value to your production. If you would like to learn more, simply contact a member of the Jordi Labs team directly.