BfArM Guidance on SAE Reporting
The article outlines the key points related to reporting serious adverse events in the context of clinical trials.
The article outlines the key points related to reporting serious adverse events in the context of clinical trials.
The final article dedicated to Diversity Action Plans describes certain specific aspects pertaining to the matter, emphasizing the key considerations.
The new article is dedicated to enrollment goals, highlighting the aspects related to the rationale behind them and the way they should be measured.
The new article pays special attention to the content of Diversity Action Plans, emphasizing the aspects related to the relevant goals.
The new article describes in detail the applicability scope and also outlines specific considerations for certain groups of patients that require special attention in order to ensure they are properly represented among study participants.
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