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CNM IRB Institutional Review Board at National College of Natural Medicine 049 SW Porter Street Portland, OR 97201 Continuing Review Form In accordance with Federal Regulations 45CFR46, the IRB must
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How to fill out continuing review form

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How to fill out a continuing review form:

01
Start by gathering all necessary information and documents required for the continuing review form. This may include previous study protocols, participant data, and any changes or updates that have occurred since the last review.
02
Begin the form by providing basic information about the study, such as the study title, Principal Investigator's name, study start and end dates, and the study site.
03
Review and update the study objectives and aims section, making sure they accurately reflect the current status of the study and any modifications that have been made.
04
Evaluate the study design and methods section, ensuring that it accurately describes the study methodology and any changes made since the last review.
05
Assess the subject population section, confirming that it includes accurate information about the populations or individuals being enrolled in the study and any changes in demographics.
06
Review the recruitment and consent process section, making sure it accurately reflects the procedures used to obtain informed consent from participants and any modifications made to these procedures.
07
Evaluate the benefits and risks section, considering any new risks or benefits that have emerged since the last review and ensuring they are appropriately addressed.
08
Assess the data collection and monitoring section, confirming that it accurately describes the methods used to collect and monitor participant data and any changes made to these methods.
09
Review the plans for data analysis and dissemination section, ensuring that it provides a clear plan for analyzing and disseminating study results and any updates to this plan.
10
Finally, sign and date the continuing review form, indicating that all information provided is accurate and up to date.

Who needs a continuing review form?

01
Researchers conducting human subjects research typically need to complete a continuing review form. This includes Principal Investigators, co-investigators, and other members of the research team who are responsible for the ongoing oversight and management of the study.
02
Institutional Review Boards (IRBs) or Ethics Committees also require a continuing review form to ensure that the study is still meeting ethical standards, participant rights are protected, and any potential risks have been mitigated.
03
Regulatory bodies, such as the Food and Drug Administration (FDA) or the Office for Human Research Protections (OHRP), may also require a continuing review form to ensure compliance with applicable regulations and guidelines for research involving human subjects.
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Continuing review form is a document that researchers submit to Ethics Committee to request approval for the continuation of their ongoing study.
Researchers who are conducting research studies that have been approved by the Ethics Committee and require periodic review.
Researchers must provide updated information on the study protocol, recruitment methods, any adverse events, and progress since the last review.
The purpose of the continuing review form is to ensure that ongoing research studies continue to meet ethical standards and protect the rights and welfare of research participants.
Researchers must report any changes to the study protocol, recruitment methods, consent forms, adverse events, and progress since the last review.
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