The impact of unannounced audits by Notified Bodies on labelling
Practical impacts of compliance with new legislation
The transition from one Notified Body to another: Strategies for scheduling and keeping track and over time
Deal with the latest regulatory changes
What will medical device manufacturers need to address?
The main impacts of the MDD Revision on medical devices labelling
Who should Attend
Document management
Marketing and communications
Technical communications
Translation
Quality assurance
Artwork
Supply chain
Technical publications
Labelling manager
Graphic design
Supply chain
Packaging
Regulatory affairs
Labelling engineer
Past Events
Labelling Compliance and UDI Implementation for Medical Devices and IVDs 2014 - 28-30 Oct 2014, Maritim Hotel Berlin, Germany (46564)
Important
Please, check "Labelling Compliance and UDI Implementation for Medical Devices and IVDs" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Medical technology
