Around the prevailing laws and regulations within the healthcare market segment, it is well known that they demand a lot from the company. It is also reasonable to establish that a patient who is ill should never, ever, be the victim of (cross) contamination and thus feel worse or have complications after taking a medicine with the aim of making him or her healthy again. This also means that much is demanded of the facility in which the various process steps take place. In Europe, Eudralex is responsible for issuing regulations and registering companies, all of which are subject to licensing, based on GMP regulations.
PP4CE has extensive experience working within those strict standards on the design and engineering process as well as the realization of cleanroom projects at any GMP level.
We have a wide range of GMP reference works such as there are:
Organon in the Netherlands, BBIO Bilthoven , Aspen Oss, Kadans Science Partner, Thermo Fisher Tilburg, VU Amsterdam, Hitma Uithoorn, AHZ The Hague, Prinses Maxima ZH Utrecht, Jansen Biologics, Catherina ZH Eindhoven, FUJI Tilburg, Repligen Breda etc.
As PP4CE, we are members of the various industry organizations and associations, such as:
ISPE/ Task Force Health Care / VCCN / FHI / NVOD / Safe Food Factory.
View the Healthcare projects here.
