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Clinical Monitoring
Clinical Quality Management
Essential Regulatory Documents
Medical Writing
Protocol Development
Protocol Deviation Reporting
SAE Reporting
Safety Oversight Committees
Study Product Information
Teleconference Support
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In your role at the clinical research site;
In the past 12 months, have you referred to the DMID Regulatory Document File Guidelines often?
Yes
Do you find the DMID Regulatory Document File Guidelines helpful?
Yes
In the past 12 months, have you referred to the DMID Source Document Standards often?
Yes
Do you find the DMID Source Document Standards helpful?
Yes
Please provide any comments in the box, below
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Created at 2/11/2019 1:27 PM by
Last modified at 2/11/2019 1:27 PM by