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EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8-001 +
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EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8-002 +
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WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 8 - Electronic data handling +
8 - Electronic data handling +
8 - Introduction +
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EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8.2-001 +
8.2 +
EU ; GBR MDCG 2020-10/1 - Safety reporting in clinical investigations of medical devices 2020 8.2-002 +
8.2 +
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