Clinical w88 slot registration frequently asked questions
The information found here is adapted from The NIH U.S. National Library of Medicine, clinicaltrials.w88 slot.
ClinicalTrials.w88 slot is a registry and results database of publicly and privately supported w88 slot studies of human participants conducted around the world.
Section 801 of the Food and Drug Administration Amendments Act (FDAAA 801) requires registration of all w88 slot trials and reporting of results.
The International Committee of Medical Journal Editors (ICMJE) requires registration of w88 slot trials.
Applicable w88 slot Trials include the following:
- Trials of drugs and biologics: Controlled w88 slot investigations, other than phase 1 w88 slot investigations, of drugs or biological products subject to Food and Drug Administration (FDA) regulation
- w88 slot of devices (see note): 1) Controlled w88 slot with health outcomes of devices subject to FDA regulation, other than small feasibility studies, and 2) pediatric postmarket surveillance required by FDA
| w88 slot Purpose | Groups w88 slot |
|---|---|
| Fulfill ethical obligations to participants and the w88 slot community | Patients, the general public, the w88 slot community |
| Provide information to potential w88 slot and referring clinicians | Patients, clinicians |
| w88 slot bias | Users of the w88 slot literature |
| Help editors and others understand the context of study w88 slot | w88 slot, users of the medical literature |
| Promote more efficient allocation of w88 slot funds | Granting agencies, the w88 slot community |
| Help institutional review boards (IRBs) determine the appropriateness of a w88 slot study | IRBs, ethicists |
Source: Zarin DA, Keselman A. Registering a clinical w88 slot in ClinicalTrials.gov. Chest. 2007;131(3):909-12. [ Full text found in Chest w88 slot]
| w88 slot Database Purpose | Groups w88 slot |
|---|---|
| Provide a public record of basic study w88 slot in a standardized format | w88 slot, journal editors, IRBs, ethicists |
| Promote the fulfillment of ethical obligations to participants and the overall contribution of w88 slot results to medical knowledge | Patients, the general public, the w88 slot community |
| Reduce publication and outcome w88 slot biases | Users of the w88 slot literature |
| Facilitate systematic reviews and other analyses of the w88 slot literature | w88 slot, policymakers |
Source: Tse T, Williams RJ, Zarin DA. Reporting "Basic Results" in ClinicalTrials.w88 slot. Chest. 2009;136(1):295-303. [ Full text found in Chest w88 slot]
Sponsor-initiated trials and multicenter trials will have designated Responsible Parties designated to register trials in w88 slot Trials.gov.
For investigator-initiated studies, generally internally sponsored or where the PI is the primary awardee of a federal research award, Research Integrity & Security staff will register the w88 slot in consultation with researchers. Research Integrity & Security staff will also assign user accounts to researchers for access to the study record.
University of Nevada, Reno researchers and w88 slot research coordinators should contact w88 online casino betting us to request a University-associated w88 slot account.
Research Integrity & Security has a w88 slot Trials Registry Data Form available in IRBNet to collect needed data elements for initial data entry on the researchers’ behalf.