Rights & Responsibilities of Research Participants
Your participation matters. Know your rights and responsibilities when joining clinical research at Pi Health Cancer Hospital.
Reach out to Pi Health to help you find the right clinical trail
Rights of Research Participants
At Pi Health Cancer Hospital, we prioritize your safety and autonomy in all research studies. Below are your fundamental rights as a research participant:
Voluntary Participation
You have the right to voluntarily participate in any research study without pressure or influence from anyone.
IEC Protection
You have the right to know about our Institutional Ethics Committee (IEC) and its role in protecting your rights and safety.
Clear Information
You have the right to receive study information in a language you understand, including purpose, procedures, risks, and benefits.
Informed Consent
You have the right to give informed consent after understanding all aspects of the study and having your questions answered.
Withdrawal Rights
You may refuse or withdraw from any study at any time without affecting your medical care or relationship with the hospital.
Quality Healthcare
You have the right to receive quality healthcare in a safe, clean environment without discrimination.
Dignified Treatment
You have the right to be treated with dignity, respect, and courtesy at all times.
Product Information
You have the right to complete information about any investigational product used in the study.
Risk Disclosure
You have the right to be informed of all risks, benefits, and alternatives of the proposed treatment.
Privacy Protection
Your personal and medical information will be kept confidential and only shared with authorized personnel.
Complaint Process
You have the right to voice complaints and know how to contact the IEC or other authorities if needed.
Responsibilities of Research Participants
While we protect your rights, we also ask that you fulfill these important responsibilities:
Provide accurate personal and medical information
Follow study protocols and procedures as instructed
Disclose complete medical history and any allergies
Adhere to treatment plans and visit schedules
Treat hospital staff with courtesy and respect
Disclose participation in other clinical trials
Avoid unauthorized medications during the study
Report any injuries or new medical conditions immediately
Ask questions when anything is unclear
Your participation is valued and essential to advancing medical research. We are committed to protecting your rights while conducting ethical, meaningful research that benefits patients worldwide.