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 Since our foundation on 1 April 1978 we have been concentrating on the pharmaceutical industry (incl. API production) and on biotechnology.
In these industries companies are obliged by law to comply with strict quality standards based on national and international regulatory guidelines like the GMP guides (Good Manufacturing Practice), providing information on quality assurance and drug safety. In these guides companies manufacturing drug products find the general requirements relative to documentation, premises, hygiene and process safety.
Regulatory Authorities strictly observe and ensure their realisation through GMP inspections and audits.
To comply with these requirements companies need highly qualified staff in all business areas. They have to know, understand and realise binding regulations – making it necessary to train staff continuously.
As Europe’s leading advanced training and information services provider
in this area CONCEPT HEIDELBERG develops and organises more than 240 seminars and conferences in 11 European countries. In addition to own events, CONCEPT HEIDELBERG also organises events on behalf of and in cooperation with various institutions – among them:
 Furthermore, our services also comprise
GMP in-house training and
GMP consulting to support pharmaceutical businesses in realising regulatory compliance on a day-to-day basis.
CONCEPT HEIDELBERG is also an associated member of the Technology Park Heidelberg
and of the
BioRN Cluster.
In 2008, the BioRN Cluster was awarded Leading-edge Cluster by the German Ministry of Education.
To learn more about CONCEPT HEIDELBERG please also see the Image Brochure which you can also
download as PDF
.
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DEUTSCH