Training: Project Management

Qserve has developed several trainings course in respect to Regulatory compliance and statutary requirements:

• CE Marking of medical devices conform to the European Medical Device Directive(s)
• Device classification
• Conformity route assessment
• Pre-clinical Testing, Clinical, Shelf life, Labeling, Packaging and Sterilization
• Design analysis by Failure Mode and Effect Analysis (FMEA) and Risk analysis methods
• Implementation of Complaint, Recall, and Vigilance systems
• Post Market Surveillance (PMS) system

These training courses are also available as in-house company training courses for groups.For more information, please complete the info request form in 'Contact Us'.