has Server used IP Address with Hostname in United States. Below listing website ranking, Similar Webs, Backlinks. This domain was first Unknown and hosted in Bethesda United States, server ping response time 17 ms

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Region: MD
City: Bethesda
Postal Code: 20817
Latitude: 39.003200531006
Longitude: -77.160202026367
Area Code: 301
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Results For Websites Listing

Found 57 Websites with content related to this domain, It is result after search with search engine PRS: Login

(5 day ago) See Submit Studies on for information on how to apply for an account, how to register your study, and how to submit results.. Send email to PRS Administration

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Go to PRS -

(4 day ago) Go to PRS. Data providers use a Web-based data entry system called the Protocol Registration and Results System (PRS) to register a clinical study or submit results information for a registered study. You must have a PRS account to register study information on If you do not have an account, see How to Apply for an Account.

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How to Register Your Study -

(6 day ago) Considerations for Observational Studies and Expanded Access Records Registering Observational Studies. The Observational Study Type (see Study Type data element on can be used to register studies of human beings in which biomedical and/or health outcomes are assessed in predefined groups of individuals, but the investigator does not assign specific interventions to the

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Register with

(4 day ago) is a consumer-friendly database with information on clinical studies funded and/or sponsored by the NIH, other federal agencies, and private industry. The database was developed by NIH, through its National Library of Medicine (NLM), in collaboration with the Food and Drug Administration (FDA).

DA: 17 PA: 50 MOZ Rank: 81 Final Rule (42 CFR Part 11) Information

(6 day ago) The Final Rule clarifies and expands the requirements for submitting clinical trial registration and results information to in accordance with Section 801 of the Food and Drug Administration Amendments Act of 2007 (FDAAA 801).The Final Rule is intended to make it clear to sponsors, investigators, and the public which trials must be reported, when they must be reported, and

DA: 26 PA: 26 MOZ Rank: 27 PRS: Login

(4 day ago) This is a test version of the Protocol Registration and Results System (PRS). Creating or modifying records in this system will have no effect on the production (operational) PRS or

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(6 day ago) HOW DO I REGISTER MY TRIAL AND REPORT RESULTS? Does the trial sponsor have an existing account with the Protocol Registration System (PRS)?The PRS is a Web-based data system that allows sponsors to submit,maintain,and update information about their trials free of charge.To find out

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Registration of Clinical Trials on

(6 day ago) December 2019. Purpose: The purpose of this guideline is to provide guidance for Johns Hopkins Medicine (JHM) investigators and study teams with clinical trials registration and results reporting on Additionally, this guideline offers guidance for posting of clinical trial consent forms for federally funded clinical trials on

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How to Register a Clinical Trial - Office of Research

(15 day ago) To register your trial on, you must have a username and password. Please submit requests for this information to the Office of Research Compliance.

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