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The agency works to ensure its GCP policies continue to facilitate new approaches to generating quality clinical evidence.</p> <h2>Latest activity</h2> <ul> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="5c5190d5-d378-46b3-8d6f-3458db355ad3" href="/regulatory-information/search-fda-guidance-documents/processes-and-practices-applicable-bioresearch-monitoring-inspections" title="Processes and Practices Applicable to Bioresearch Monitoring Inspections">Processes and Practices Applicable to Bioresearch Monitoring Inspections</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="69af073d-dd6b-4265-a3d7-62ea2fbf33e1" href="/regulatory-information/search-fda-guidance-documents/conducting-clinical-trials-decentralized-elements" title="Conducting Clinical Trials With Decentralized Elements">Decentralized Clinical Trials for Drugs, Biological Products, and Devices</a></li> <li><a data-entity-substitution="canonical" 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Investigators, and Other Stakeholders</li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="7be81cbf-d4dd-45c4-96cc-44bdd2ea1265" href="/news-events/press-announcements/fda-takes-action-failure-submit-required-clinical-trial-results-information-clinicaltrialsgov" title="FDA Takes Action For Failure to Submit Required Clinical Trial Results Information to ClinicalTrials.Gov">FDA Takes Action For Failure to Submit Required Clinical Trial Results Information to ClinicalTrials.Gov</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="387458d4-3684-4613-be82-dc90655e3bcc" href="/regulatory-information/search-fda-guidance-documents/civil-money-penalties-relating-clinicaltrialsgov-data-bank" title="Civil Money Penalties Relating to the ClinicalTrials.gov Data Bank">FDA Publishes Guidance on Civil Money Penalties Relating to the ClinicalTrials.gov Data Bank (August 2020)</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="0eb51ac5-c567-494a-a1c5-15cc8cfec365" href="/regulatory-information/search-fda-guidance-documents/institutional-review-board-irb-review-individual-patient-expanded-access-submissions-investigational" title="Institutional Review Board (IRB) Review of Individual Patient Expanded Access Submissions for Investigational Drugs and Biological Products">FDA Publishes Guidance on Institutional Review Board Review of Individual Patient Expanded Access Requests for Investigational Drugs and Biological Products During COVID-19 Public Health Emergency</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="f3e5e439-cf8d-4945-a87a-66fc82e74e6a" href="/about-fda/page-not-found">FDA issues Guidance on Conduct of Clinical Trials of Medical Products During the COVID-19 Pandemic</a></li> </ul> <h2>Bioresearch monitoring</h2> <div class="aside"><a class="btn btn-block btn-primary" data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="105de180-f098-49b9-b3fb-09abcc0e8859" href="/inspections-compliance-enforcement-and-criminal-investigations/compliance-program-manual/bioresearch-monitoring-program-bimo-compliance-programs" title="Bioresearch Monitoring Program (BIMO) Compliance Programs">View BIMO Compliance Programs</a></div> <p><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="6a9fd227-e4b5-4f8d-a6ea-b8f793186a0f" href="/inspections-compliance-enforcement-and-criminal-investigations/compliance-actions-and-activities/fda-bioresearch-monitoring-information" title="FDA Bioresearch Monitoring Information">FDA鈥檚 bioresearch monitoring (BIMO) program</a> is a comprehensive program of on-site inspections and data audits designed to monitor all aspects of the conduct and reporting of FDA-regulated research.</p> <h2>Workshops, meetings, and conferences</h2> <ul> <li><a href="https://www.socra.org/conferences-and-education/training-conferences-workshops-courses/fda-clinical-trial-requirements-regulations-compliance-and-gcp-conference/program-information/" target="_blank">Conferences</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="df7c36b3-736a-4d55-940e-f03bd4b2ba08" href="/science-research/clinical-trials-and-human-subject-protection/workshops-and-meetings" title="Workshops and Meetings">Workshops and meetings</a></li> </ul> <h2>Contacts</h2> <ul> <li>Good clinical practice: <a href="mailto:gcpquestions@fda.hhs.gov">gcpquestions@fda.hhs.gov</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="d057f9b5-8c5a-4bb5-9af5-25141c72cfcb" href="/science-research/clinical-trials-and-human-subject-protection/indide-contacts" title="IND/IDE Contacts">IND/IDE contacts</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" 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Trials">Reporting complaints related to FDA-regulated clinical trials</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="011a5033-6b54-472a-afbe-46c31f91db36" href="/science-research/report-problems-fda/mandatory-irb-reporting-fda-contacts" title="Mandatory IRB Reporting: FDA Contacts">Mandatory IRB reporting: FDA contacts</a></li> </ul> <h2>Resources</h2> <ul> <li><a href="/science-research/clinical-trials-and-human-subject-protection/clinical-trial-forms">Clinical trial forms</a></li> <li><a href="http://clinicaltrials.gov/ct2/home" target="_blank">ClinicalTrials.gov (NIH)</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="2648dda7-4ed9-4fd1-8cbd-7d45e58245ba" href="/about-fda/office-chief-medical-officer/office-clinical-policy" title="Office of Clinical Policy">Office of Clinical Policy</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="b7332514-27c4-4653-8ab3-db29150c47af" href="/regulatory-information/dockets-management" title="Dockets Management">Dockets management</a></li> <li><a data-entity-substitution="canonical" data-entity-type="node" data-entity-uuid="1b868094-4a46-47fb-824d-a085aac05813" href="/news-events/approvals-fda-regulated-products" title="Approvals of FDA-Regulated Products">Approvals of FDA-Regulated Products</a></li> </ul> <br> <br> </div> <aside class="col-md-2 col-md-push-2" role="complementary"> <section id="block-entityviewcontent-4" data-block-plugin-id="entity_view:node" class="block block-ctools block-entity-viewnode clearfix"> <div class="region region-"> <aside class="lcds-card lcds-card--border-top" > <ul role="menu" class="lcds-description-list"> <li role="menuitem" class="node-current-date lcds-description-list__item"> <div> <h2 class="lcds-description-list__item-heading">Content current as of:</h2> <p class="lcds-description-list__item-text"><time 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