Get the free ClinicalTrials.gov Final Rule (42 CFR Part 11) Information
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Testing the Efficacy of an Online Integrated Treatment for Comorbid Alcohol Misuse and
Emotional Problematics Amendment Approved February 28th, 2018Informed Consent Former. Matthew Keogh, Ph.D.
University
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Who needs clinicaltrialsgov final rule 42?
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Clinical researchers, investigators, and study sponsors involved in conducting clinical trials need to comply with clinicaltrialsgov final rule 42. It is a regulatory requirement for transparency and public access to clinical trial information. Compliance with this rule ensures the disclosure of key information about the trial, including study design, protocol details, recruitment status, and results. It helps to increase transparency, accountability, and accessibility of clinical trial data for the benefit of the research community, healthcare professionals, and the general public.
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What is clinicaltrialsgov final rule 42?
The clinicaltrialsgov final rule 42 refers to the final rule issued by the National Institutes of Health (NIH) requiring registration and reporting of clinical trials.
Who is required to file clinicaltrialsgov final rule 42?
All sponsors or investigators conducting clinical trials are required to file clinicaltrialsgov final rule 42.
How to fill out clinicaltrialsgov final rule 42?
To fill out clinicaltrialsgov final rule 42, sponsors or investigators need to provide detailed information about the clinical trial, including protocol details, participant enrollment, and results.
What is the purpose of clinicaltrialsgov final rule 42?
The purpose of clinicaltrialsgov final rule 42 is to promote transparency and accountability in clinical research by making information about clinical trials publicly available.
What information must be reported on clinicaltrialsgov final rule 42?
Information such as trial protocol details, participant recruitment status, and trial results must be reported on clinicaltrialsgov final rule 42.
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