Courses
super-compact (~2h duration), delivered to you Live or via video Conference
Q2 2024 courses are now fully booked
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Audit and Inspection Management
Preparations that lead to success. Do’s and dont’s during an Health Authority Inspection or Audit.
Good Clinical Practice for Managers
Clinical studies will need to adhere to revised ICH GCP Guidelines, if the product is to be marketed in EU, US or Japan.
Quality Assessment of 3rd party subcontractors
Find the weak spots of your potential 3rd party service supplier, before it’s too late.
Emergency management in Pharma companies
Learn how to efficiently manage and prepare for a potential company crisis.
The EU General Data Protection Regulation in clinical trials
Get updated on the EU latest development with regard to Informed Consent on Personal Data.
The EU Clinical Trials Regulation No 536/2014
How to get your trial started now when the new EU regulation is effective.