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Eudralex Volume 10 Detailed guidance on the request to the competent authorities for authorisation of a clinical trial on a medicinal product for human use, the notification of substantial amendments and the declaration of the end of the trial (CT-1)
Short Title:
2010/C 82/01
Origin/Publisher:
European Commission
Document Type:
Communication
Content:
request to the competent authorities for authorisation of a clinical trial on a medicinal product for human use, the notification of substantial amendments and the declaration of the end of the trial
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