Adherence to Good Manufacturing Practice requirements (GMPs) is of fundamental importance for the pharmaceutical industry. GMP requires that manufacturers or distributors operating in domestic or international markets have an adequate Quality Systems for the manufacture, testing, packaging, labelling, storage and distribution of medicinal products in place. A Qualified Person is required for the quality oversight and release of your products to the European market.

This system should ensure that the drug products are adequately safe and effective for their intended use and meet the required quality and purity characteristics.

We support you to establish these requirements in a way that fits with your company’s needs.