Vigilance and Product Recall
New Guidance for Manufacturer's and European Representatives of Medical Device and In-Vitro Diagnostic Medical Devices
Vigilance and Product Recall
All suppliers and manufacturer's of CE Marked Products in the Medical Device and In-Vitro Diagnostic Medical Device Sectors need to take notice of updated European Guidelines for Vigilance and Product Recall.
This is not such a bad thing as is clearly defines what is and is not a product recall and in many instances actually makes a recall less likely.
What it does do however is place greater emphasis on ensuring staff are familiar with the updated information as there is now no excuse not to recall products if the criteria is met.
This is not such a bad thing as is clearly defines what is and is not a product recall and in many instances actually makes a recall less likely.
What it does do however is place greater emphasis on ensuring staff are familiar with the updated information as there is now no excuse not to recall products if the criteria is met.
