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Protocol Version Date: December 3, 2019PBTC055 Page 1 of 18Research Study Informed Consent Document for PBTC055 Phase I Stratum 2 Study Title for Participants: Testing the benefit of adding to trametinib
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01
Begin by reading the research study informed consent form carefully.
02
Make sure you understand all the information provided in the form.
03
Fill out the personal information section, including your name, contact details, and any other required details.
04
Read through the study's objectives, procedures, potential risks, and benefits.
05
If you have any questions or concerns, discuss them with the researcher or study coordinator before signing the form.
06
Once you feel comfortable and satisfied, sign and date the informed consent form.
07
Keep a copy of the consent form for your records.
08
Make sure you fully comprehend your rights as a participant and the steps involved in the study.

Who needs research study informed consent?

01
Anyone who wishes to participate in a research study needs to have a research study informed consent form.
02
This ensures that participants are well-informed about the study, its procedures, potential risks, and benefits, and gives them the opportunity to voluntarily decide whether or not to participate.
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Research study informed consent is a process in which individuals are given important information about a research study before deciding whether to participate. This information helps participants make an informed decision about their involvement.
Researchers conducting a study are required to obtain informed consent from participants before conducting any research activities.
The process of filling out a research study informed consent form typically involves providing information about the study purpose, procedures, risks and benefits, confidentiality, and the participant's rights. Participants are then asked to sign the form to indicate their consent.
The purpose of research study informed consent is to ensure that participants understand the nature of the research study, what will be required of them, and any potential risks or benefits involved. This helps protect participants' rights and ensures ethical conduct in research.
Research study informed consent forms typically include information about the study purpose, procedures, risks and benefits, confidentiality, the participant's rights, and contact information for questions or concerns.
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