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This informed consent form provides details regarding a prospective, multi-center, randomized, open, parallel-controlled clinical study aimed at evaluating the effectiveness and safety of BD Pre-filled Flush Syringes made by BD Medical Technology (Jiangsu) Co., Ltd., in comparison to those manufactured by BD, USA. It outlines participant rights, study procedures, potential risks, and benefits associated with participation.
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How to fill out informed consent form
How to fill out informed consent form
01
Read the entire form carefully before starting.
02
Provide your personal information in the designated sections.
03
Clearly understand the study or procedure, including risks and benefits.
04
Ask questions if any part of the form or study is unclear.
05
Sign and date the form where indicated.
06
Keep a copy of the signed consent form for your records.
Who needs informed consent form?
01
Participants in clinical trials.
02
Patients undergoing medical procedures or treatments.
03
Individuals involved in research studies.
04
Parents or guardians of minors participating in studies.
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What is informed consent form?
An informed consent form is a document that provides potential participants with detailed information about a study, including its purpose, procedures, risks, benefits, and their rights, allowing them to make an informed decision about their participation.
Who is required to file informed consent form?
Researchers conducting studies involving human subjects are required to file informed consent forms to ensure participants are fully informed about the study.
How to fill out informed consent form?
To fill out an informed consent form, researchers should provide clear and understandable information, include participant rights, ensure the person providing consent is aware of what they are consenting to, and have the participant sign and date the form.
What is the purpose of informed consent form?
The purpose of an informed consent form is to protect the rights and welfare of participants by ensuring they are fully aware of the study's nature, risks, benefits, and their ability to withdraw at any time.
What information must be reported on informed consent form?
The informed consent form must include the study's purpose, procedures, duration, risks, benefits, confidentiality assurances, contact information for questions, and a statement about voluntary participation and withdrawal rights.
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