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Annex 2 Informed consent FOR PARTICIPATION IN CLINICAL RESEARCH PROTOCOLS FACULTY OF MEDICINE UNIVERSITY DE ANTIOQUIAProject title: Nontechnical skills training and checklists versus standard training
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Start by downloading the PDF research ethics committee form from the relevant website or institution.
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Open the PDF form using a PDF reader or editor software.
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Read the instructions provided with the form thoroughly to understand the requirements and guidelines for filling it out.
04
Begin filling out the form by entering the necessary information such as the researcher's name, contact details, and institutional affiliation.
05
Provide a clear and concise title for the research project in the designated field.
06
Fill in the details about the research methodology, including the purpose, design, and procedures involved.
07
Clearly outline the target population and explain the process of participant selection.
08
Describe any potential risks or ethical considerations associated with the research and the steps taken to minimize them.
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Attach any required supporting documents, such as consent forms or research protocols, according to the instructions provided.
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Review the completed form to ensure all information is accurate and complete.
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Save a copy of the filled-out form for your records, and if required, submit the form electronically or through the designated submission process.
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Follow any additional instructions or requests for revisions provided by the committee until the process is completed.

Who needs pdf research ethics committees?

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Researchers, scientists, and academics who are planning to conduct research involving human subjects or sensitive data are typically required to submit their research proposals to research ethics committees.
02
Institutional review boards (IRBs) or independent ethics committees are responsible for ensuring that research studies adhere to ethical standards, protect the rights and well-being of the participants, and comply with legal and regulatory requirements.
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These committees are commonly found in universities, research institutions, healthcare organizations, and other entities involved in research.
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PDF research ethics committees review and approve research involving human subjects to ensure ethical standards are met.
Researchers conducting studies with human subjects are required to file PDF research ethics committees for approval.
To fill out PDF research ethics committees, researchers need to provide detailed information about the study protocol, risks, benefits, and informed consent procedures.
The purpose of PDF research ethics committees is to protect the rights and welfare of human subjects participating in research studies.
Researchers must report detailed information about the study design, procedures, risks, benefits, and informed consent process on PDF research ethics committees.
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