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Disclaimer:The information presented in these works draws upon the combined understanding and knowledge of the eClinical Forum and is provided as an aid to understanding the environment for electronic clinical research. The opinions of the author(s) and the eClinical Forum do not necessarily reflect the position of individual companies.The content is unconfirmed and users should assess the content and opinions in the light of their own knowledge, needs and experience as well as interpretation of relevant guidance and regulations.

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Members Release: Best Practice Document on Investigator’s Signature Members Release: Best Practice Document on Investigator’s Signature
The eClinical Forum is happy to announce the release of the "Investigator’s signature on electronic Case Report Forms (eCRFs), MR2022”. About the Best Practice Document: There is increased scrutiny by regulatory agencies on the...

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eCF Requirements for Electronic Data for Regulated Clinical Trials PR2021 eCF Requirements for Electronic Data for Regulated Clinical Trials PR2021
The eClinical Forum is happy to announce the Public release of the "eCF Requirements for Electronic Data for Regulated Clinical Trials PR2021" ABOUT THE ECF REQUIREMENTS:  The eClinical Forum has produced a set of Requirements,...

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