G+H provides automated solutions which are validated according to the GMP standards. The safety requirements are very significant when delivering process technology for production of medicine to the pharmaceutical industry.

To prove that production conditions and quality control complies with current requirements, the process and support facilities in this industry are validated according to GPM (Good Manufacturing Practice) standards. GPM demands high requirements for documentation, test procedures, and proving that the test procedure has been performed with the desired result. For Statens Serum Institut G+H has delivered solutions validated according to the GMP requirements.

Statens Serum Institut is a public enterprise operating as a market-oriented production and service enterprise.
Statens Serum Institut is an enterprise under the Danish Ministry of Health and Prevention, and the Institute’s duties are partly integrated in the national Danish health services.