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Eudralex Volume 10 Detailed guidance on the collection, verification and presentation of adverse event/reaction reports arising from clinical trials on medicinal products for human use (‘CT-3’

Short Title:
Detailed guidance on the collection, verification and presentat
Origin/Publisher:

Official Journal of the European Union

Document Type:
Guidance
Content:
Detailed guidance on the collection, verification and presentation of adverse event/reaction reports arising from clinical trials on medicinal products for human use (‘CT-3’)

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