Continuing Education to GxP Compliance
A lot of aspects are to be kept into consideration when trying to comply with regulatory requirements to name but a few:
- profound knowledge of guidelines, directives regulations etc.
- interpretation and realisation of regulatory requirements
- excellent planning quality for conductance of clinical trials in total (and not only with the IMP supply chain)
- intensive communication between internal "customer" and internal "supplier"
- pro-active readiness for cooperation and collaboration between all parties involved into preparation of IMPs;
Concepts necessary for realisation of such optimal processes are available with us and ready for implementation !
Whatever kind of training you need
- open and public trainings
- in-house trainings
- intensive coachings
- web-basied training
- blended learning or even
- audio books
we will be happy to constructively identify your company specific needs and tailor the respective programme together with you !