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Large Language Model-Enabled AE Identification In Scientific Publications
Can a commercial LLM and custom prompts summarize abstracts and full-text articles to identify adverse events for human review?
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Community leadership announces merger of DIA GCP & QA and Clinical Research to form new Clinical Research, Compliance, and Quality Community.

DIA-MHRA Global Summit
Developed in partnership with the UK’s Medicines and Healthcare products Regulatory Agency (MHRA), this inaugural gathering will showcase how the UK enables innovation across the full pathway—from early development and clinical investigation to regulation, evidence generation, and real-world adoption.
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全球论坛,DIA数字杂志

网罗医疗保健产品在全球以及区域范围内发现、开发、监管、监督、营销方面的专家观点,涵盖思想领袖的采访与教育活动的专题摘要。

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