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NHS REC Research Tissue Bank (RTB) FormReference: 11/NW/0382IRAS Version 3.1 WelcometotheIntegratedResearchApplicationSystem IRASProjectFilter Theintegrateddatasetrequiredforyourprojectwillbecreatedfromtheanswersyougivetothefollowingquestions.
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To fill out the NHS REC research database, follow these steps:
02
Access the NHS REC research database website.
03
Register an account or log in if you already have one.
04
Click on the 'Submit New Research' button.
05
Fill in the required fields such as research title, description, study type, start and end dates, etc.
06
Provide any additional information or documents required by the database.
07
Review your submission for any errors or missing information.
08
Click on the 'Submit' button to complete the process.
09
Wait for the database administrators to review and approve your research entry.
10
Keep track of any communication or updates regarding your submission.

Who needs nhs rec research database?

01
The NHS REC research database is needed by researchers, healthcare professionals, and organizations involved in conducting and publishing healthcare-related research.
02
It is a valuable resource for storing and sharing research findings, improving collaboration, and ensuring transparency in the research process.
03
Regulatory bodies, funding agencies, and policy-makers may also utilize the database to evaluate the quality and impact of healthcare research.
04
Furthermore, patients and the general public can benefit from the database by accessing reliable information on ongoing research studies and their potential implications.
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NHS REC Research Database is a centralized system used for tracking and managing research projects approved by the National Health Service Research Ethics Committee.
Researchers conducting studies approved by the National Health Service Research Ethics Committee are required to file information on the NHS REC Research Database.
Researchers can fill out the NHS REC Research Database by providing detailed information about their research projects, including study objectives, methodology, participants, and outcomes.
The purpose of the NHS REC Research Database is to ensure transparency, accountability, and compliance with ethical standards in research conducted within the National Health Service.
Researchers must report detailed information about their research projects, including study protocol, informed consent procedures, data collection methods, and any potential risks or benefits for participants.
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