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Even though a participant may not be asked for his/her name in the survey other pieces of information IP address email address zip code etc. and/or demographic questions sex and race especially in a small sample with low diversity can potentially be used to glean the identity of individual participants. Rutgers University. Web. 6 Jan. 2016. http //comminfo. rutgers. edu/ cgal/IRB. pdf. are securely housed in an on-site limited access data center managed by name of institution s department...
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Step 1: Obtain a copy of the informed consent resource library template.
02
Step 2: Review the template to understand the required sections and information.
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Step 3: Identify the specific details related to the study or research project.
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Step 4: Fill out the general information section, including the project title, principal investigator's name, and contact information.
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Step 5: Provide a detailed description of the study or research project, including the purpose, procedures, potential risks, and benefits.
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Step 6: Include any additional information or appendices required to ensure participants have all necessary details.
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Step 7: Clearly explain the voluntary nature of participation and the right to withdraw at any time without consequences.
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Step 8: Include language that ensures the confidentiality and privacy of participants' personal information.
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Step 9: Provide space for participants to sign and date the consent form, indicating their informed agreement.
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Step 10: Review the completed informed consent resource library for accuracy and completeness before using it with participants.

Who needs informed consent resource library?

01
Researchers conducting studies or projects involving human participants.
02
Scientific institutions, universities, and research organizations.
03
Ethics review boards and committees responsible for approving research protocols.
04
Healthcare professionals and medical practitioners involved in clinical trials.
05
Organizations or individuals undertaking social or behavioral research.
06
Educational institutions performing research involving students or participants.
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Any project or study that requires informed consent to ensure ethical and legal compliance.
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The informed consent resource library is a collection of documents and information used to educate individuals about a specific topic or procedure before obtaining their consent.
Any organization or individual that is involved in obtaining informed consent from individuals is required to maintain and file an informed consent resource library.
To fill out an informed consent resource library, you must gather all relevant documents and information, organize them in a systematic way, and ensure they are easily accessible for reference.
The purpose of the informed consent resource library is to ensure that individuals have access to relevant information before giving their consent to a specific procedure or activity.
The informed consent resource library must include all relevant documents, information about the procedure or activity, potential risks and benefits, alternative options, and any other details necessary for individuals to make an informed decision.
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