Participant Rights & Responsibilities

Part A

Your Rights as a Participant

These rights apply to every participant in every study at our Clinical Research Centre — before you join, while you take part, and if you decide to leave.

RIGHT 01

Free choice

You may decide freely whether to join a clinical trial.

RIGHT 02

Leave at any time

You may withdraw at any time without affecting your regular medical care.

RIGHT 03

Clear information

You will receive clear information about the study purpose, procedures, risks, benefits, and alternatives.

RIGHT 04

Ask questions

You may ask questions at any time and receive understandable answers.

RIGHT 05

Consent first

Your written consent will be taken before any study-related procedure.

How consent works →
RIGHT 06

Safety & care

Your safety will be monitored, and care will be provided for study-related injury as applicable.

RIGHT 07

Confidentiality

Your personal and medical information will be kept confidential.

RIGHT 08

Ethics oversight

The study is approved and monitored by an Ethics Committee.

RIGHT 09

Dignity & respect

You will be treated with dignity and respect at all times.

Part B

Your Responsibilities

Your study doctor relies on accurate, timely information from you. These responsibilities help the team look after your health and keep the study results reliable.

Tell the study team promptly if you have:

  • Any discomfort or side effects
  • A new illness or hospitalization
  • Started any new medicines
  • A scheduled visit you cannot attend
My participant checklist0 / 6
Tick each item to confirm you understand it. Nothing is saved or sent.
“Your rights come first. Your participation helps bring better treatments to future patients.”

Clinical Research Centre · KG Hospital

Resources

Have a Question?

Speak to your study doctor or the Clinical Research Centre team at any time. You can also download this guide in English or Tamil.

Download (English PDF) தமிழ் (PDF) Informed Consent Process Phases of Clinical Trials Contact the Team