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Good Manufacturing Practice (GMP) ensures consistence production process and product control in accordance with international quality standards.
GMP – is a global quality standard for the production of medicines, designed to reduce the risks of using any pharmaceutical product and is mandatory for all EU member states.
Compliance with GMP requirements is the best way to do business that put quality first.
GMP services
Audit of pharmaceutical companies-manufacturers for compliance with the requirements of good manufacturing practice (GMP), conducting expert work and providing advice on good manufacturing practice (GMP);
Audit of manufacturers of active pharmaceutical ingredients (API) for compliance with the requirements of good manufacturing practice (GMP);
Corporate training of your company’s staff on GMP issues;
Development of a corrective and preventive action plan (CAPA) to ensure compliance, as well as advisory support in the implementation of the CAPA plan.
GXP’s mission – to facilitate the process of medical devices legalization and to create a legal way for new players to enter the EU and CIS market of medical devices, which in general will lead to qualitative changes in the market.
ul.Lubicz 27/40, 31-503
Krakow, Poland
+48 1225 44 831
+48 6906 25 630
info@gxp-europe.com
We are a team of experts with a broad experience in medical devices (MD) regulation (MD), good manufacturing practice (GMP), good distribution practice (GDP). We know irreproachably requirements of the national and European legislation.
ul.Lubicz 27/40, 31-503
Krakow, Poland
+48 1225 44 831
+48 6906 25 630
info@gxp-europe.com
GXP ©Copyright. All rights reserved