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Annexure-I INFORMED CONSENT FORM STUDY TITLE: PRESCRIPTION DRUG ERRORS IN ANAND DISTRICT DOCTOR? S NAME: I have been explained regarding the research project ?PRESCRIPTION DRUG ERRORS IN ANAND DISTRICT?
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An informed consent form is a document that outlines the details of a medical procedure or research study, ensuring that participants are fully aware of the risks, benefits, and alternatives before agreeing to proceed.
Researchers and healthcare providers who conduct medical procedures or clinical trials are required to file informed consent forms to protect the rights and welfare of participants.
To fill out an informed consent form, a participant should read the entire document carefully, ask questions for clarification, and then provide their signature and date to indicate their agreement to participate.
The purpose of an informed consent form is to ensure that individuals understand what they are consenting to, enabling them to make educated decisions about their participation in research or treatment.
The informed consent form must report information such as the purpose of the study or procedure, the duration, potential risks, benefits, and alternative options, as well as confidentiality protections and the right to withdraw at any time.
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