Below are links to other regulatory research policies.
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NIH Guidance on New Law (Public Law 110-85) Enacted to Expand the Scope of ClinicalTrials.gov: Registration
This outlines application, scope and responsibility of trial registration under the FDAAA.
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Food and Drug Administration Amendments Act of 2007 (FDAAA)
This law ensures that FDA staff have the resources needed to conduct the complex and comprehensive reviews necessary to new drugs and devices. Among the many components of the law, the Prescription Drug User Fee Act (PDUFA) and the Medical Device User Fee and Modernization Act (MDUFMA) have been reauthorized and expanded.
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ClinicalTrials.gov
A international registry of federally and privately supported clinical trials, it provides information about a trial's purpose, who may participate, locations, and phone numbers for more details. Use the Contact Information to obtain an access code to the UK Organizational Account on ClinicalTrials.gov.
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Physician Data Query Cancer Clinical Trials Registry
To help ensure the comprehensiveness of the registry, PDQ© and NIH's ClinicalTrials.gov database regularly exchange clinical trial information. Cancer trials registered in PDQ© will automatically be registered in ClinicalTrials.gov and vice versa.
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World Health Organization International Clinical Trials Registry Platform
Its mission is to ensure that a complete view of research is accessible to all those involved in health care decision making.
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