Safety Features for Medicinal Products for Human Use Questions and Answers Version 12

This slide deck addresses Safety Features for Medicinal Products for Human Use (version 12) prepared by the European Commission Directorate-General for Health and Food Safety.  Questions focus on requirements for Unique Identifier, Safety Features, Repository systems, and obligations of importers/wholesalers/and distributors.  The answers found in this document provide specific guidance for these questions.  Please review the questions and access resource links for detailed answers.

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