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11.07.2017Submission of comments on 'Guideline on GCP compliance in relation to trial master file (paper and/or electronic) for content, management, archiving, audit and inspection of clinical trials
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The purpose of submission of comments on is to gather different perspectives, feedback, and insights on a particular topic to make informed decisions.
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The information that must be reported on submission of comments on includes the name of the individual or organization submitting the comments, contact information, the actual comments or feedback, and any supporting documentation.
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