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NORTH Ethics Committee for Clinical Studies 8.3 Management of Study TerminationTitle: Management of Study Termination SOP Code: SOP/18/V1.1Effective date: 24/09/2014SOP Code: SOP/18/V1.1 Effective
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01
To fill out NIRRH Ethics Committee form, follow these steps:
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Start by obtaining the NIRRH Ethics Committee form from the NIRRH website or the relevant authority.
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Read the instructions carefully and gather all the necessary documents and information needed to complete the form. This may include research proposals, consent forms, participant information sheets, and any relevant supporting materials.
04
Fill in the required personal and contact details in the designated sections of the form, such as name, address, email, and phone number.
05
Provide a detailed description of the research project, including its objectives, methodology, and expected outcomes. Be concise and clear while explaining the research design and procedures.
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Ensure you provide an ethical justification for the proposed research, describing how it aligns with the principles of human research ethics and the protection of participant rights.
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Declare any potential conflicts of interest or funding sources that might influence the research process or outcomes.
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If applicable, outline the participant recruitment process, inclusion/exclusion criteria, and strategies for ensuring informed consent and confidentiality.
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Submit the completed form along with all the supporting documents to the NIRRH Ethics Committee.
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Await confirmation or further instructions from the committee regarding the approval status of your research proposal.
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Note: It is crucial to familiarize yourself with the specific guidelines and requirements of the NIRRH Ethics Committee before filling out the form to ensure compliance with their protocols.

Who needs nirrh ethics committee for?

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The NIRRH Ethics Committee is required by individuals or organizations conducting research involving human participants in the field of reproductive health and related areas.
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Some examples of who needs NIRRH Ethics Committee approval include:
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- Researchers conducting clinical trials or studies on reproductive health interventions, contraceptives, infertility treatments, or assisted reproductive technologies.
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- Medical professionals engaged in research on maternal and child health, family planning, genetics, or sexually transmitted infections.
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- Students or scholars undertaking research projects that involve human participants and fall within the purview of the NIRRH's research focus areas.
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It is advisable to consult the NIRRH Ethics Committee guidelines or contact them directly if there are any doubts about whether your research requires their approval.
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The NIRRH Ethics Committee is responsible for reviewing and approving research studies involving human participants to ensure they adhere to ethical standards and guidelines.
Researchers conducting studies involving human participants are required to submit their research proposals to the NIRRH Ethics Committee for review and approval.
Researchers need to submit their research proposals, along with all relevant documentation and consent forms, to the NIRRH Ethics Committee for review in order to complete the form.
The purpose of the NIRRH Ethics Committee is to protect the rights, safety, and well-being of research participants by ensuring that research studies are conducted ethically.
Researchers must report details of their study design, participant recruitment methods, informed consent procedures, potential risks, and benefits, as well as data management and confidentiality measures.
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