The European Commission has published an updated version, Version 19, of the Questions and Answers document on the Safety Features for Medicinal Products for Human Use.
Version 19 of the document, dated December 2021, supersedes Version 18. Q&A 1.29 was added, while Q&As 1.22, 5.8 and 7.19 were revised.
More information is available on the Commission’s website.
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