Canada
The new article clarifies the reporting requirements associated with medical device recalls and explains the key terms and concepts used in this respect.
DRAP
The new article describes in detail the recall procedure to be followed when removing defective products from the market to ensure the safety of patients.
DRAP
The new article provides an overview of the critical responsibilities of the parties involved in recalls associated with therapeutic products, as well as additional communication details to ensure the vitally important safety information is duly delivered to the affected parties.
DRAP
The new article highlights certain specific aspects related to the recalls the parties responsible for medical devices should initiate once it is identified that such products may pose risks to public health.
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