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GHANA HEALTH SERVICE ETHICS REVIEW COMMITTEE CONTINUING REVIEW SUBMISSION Requirements: +2330302681109/ 2330302679323/ Fax + 2330302685424 Email: fierce×Gmail.comas stated in the Standard Operating
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How to fill out continuing review submission requirements

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How to fill out continuing review submission requirements

01
To fill out continuing review submission requirements, follow these steps:
02
Review the regulatory requirements and guidelines specific to your jurisdiction or institution.
03
Gather all the necessary documents and information related to the study that requires continuing review.
04
Ensure that all the submitted documents are up to date, including informed consent forms, study protocols, and any amendments.
05
Complete the continuing review submission form provided by your institution or regulatory authority.
06
Provide a detailed progress report of the study, including recruitment status, participant demographics, adverse events, and any changes made to the study protocol.
07
Include any interim results or findings from the study if applicable.
08
Pay attention to any specific requirements for reporting and deadlines set by your institution or regulatory authority.
09
Submit the completed continuing review submission and all supporting documents through the designated submission portal or to the appropriate authority.
10
Keep records of the submission confirmation and any correspondence related to the continuing review process.
11
Respond promptly to any requests for additional information or clarifications from the reviewing authority.
12
Follow any instructions or recommendations provided by the review board or authority regarding the continuation or modifications to the study.
13
Maintain regular communication with the relevant stakeholders throughout the continuing review process.

Who needs continuing review submission requirements?

01
Continuing review submission requirements are typically needed by researchers and institutions involved in human subjects research studies.
02
It is a regulatory process that ensures the ongoing safety, ethical considerations, and scientific validity of the study.
03
Researchers conducting clinical trials, observational studies, or any research involving human participants usually need to submit continuing review requirements.
04
Institutions such as universities, medical centers, research organizations, or ethics committees often mandate the submission of continuing review materials.
05
These requirements help to protect the welfare and rights of participants and maintain compliance with ethical standards and applicable regulations.

What is CONTINUING REVIEW SUBMISSION REQUIREMENTS Form?

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Continuing review submission requirements involve the submission of a progress report to the Institutional Review Board (IRB) to ensure that the research study is still being conducted ethically and within regulatory guidelines.
Principal Investigators (PIs) and research teams conducting human subjects research are typically required to file continuing review submission requirements.
Continuing review submission requirements can be completed by providing updated information on the progress of the research study, any changes in the protocol, and any adverse events that have occurred.
The purpose of continuing review submission requirements is to ensure the ongoing safety and welfare of human subjects participating in research studies and to maintain compliance with regulatory standards.
Information that must be reported on continuing review submission requirements includes updates on the research study progress, any protocol modifications, adverse events, and any other relevant information.
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