Europharm offers GMP or GDP compliance audit services ensuring that high standards of Quality Management in the development, manufacture and control of medicinal products are maintained. Whether the products are sold within or outside of the European Union, all pharmaceutical manufacturers in the Union require manufacturing authorisations ensuring the compliance with contemporary requirements of safety, quality and efficacy.
GDP is a specific section of the drug development, manufacturing and sales processes. The main aim is to maintain integrity of the products during transportation and storage stages of the drug manufacture and distribution processes.
We support our clients in fully complying with GMP/GDP and similar guidelines with maximum efficiency and accuracy.