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Document: Business process description for pharmacovigilance-2025/10/29
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Page: What we publish on medicines and when-2025/10/29
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Page: Plasma master file certificates-2025/10/28
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Page: Advanced therapy classification-2025/10/28
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Document: Article 57 product data-2025/10/28
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Document: Agenda - ACT EU multi-stakeholder platform annual meeting - October 2025-2025/10/28
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Page: Pre-authorisation guidance-2025/10/28
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Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure-2025/10/28
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Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2025/10/28
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Document: Template for sharing EMA documents by Industry to support reliance-2025/10/28
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