volunteer registration - Syngene International Ltd

FAQ

Volunteers Needed

Syngene is recruiting healthy volunteers for paid clinical trials. Join us today!

Syngene International Ltd. is one of the leading clinical research organization’s (CRO) in India. We conduct clinical trials with the help of paid volunteers to aid the development of new medicines on behalf of the world’s leading pharmaceutical and biotechnology companies.

Why should you consider volunteering for clinical trials?

We are seeking volunteers for sponsored clinical trials in Bangalore. Volunteers are the backbone of clinical trials, providing the essential data needed to evaluate the safety and effectiveness of new therapies. By joining, you contribute to medical breakthroughs that can improve and save lives. Your involvement not only aids in scientific discovery but also supports the health and well-being of future generations. If you are interested in making a difference, please consider volunteering for these trials.

Please note: Volunteers will be compensated, and their data kept confidential and secure per Govt. of India, New Drugs and Clinical Trials Rules, 2019.

Contact details:

8884219666 / 9606950650

Syngene International Ltd., Semicon park, Human Pharmacology Unit
(Map Location)

Please share your details to register now

Enter your Name *

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By submitting this form, you authorise Syngene to keep your personal information on Syngene’s clinical trial/ research volunteer database, so we can contact you about the clinical trials/ research studies that we conduct. All your personal information will be treated confidential by Syngene. Syngene will not share your information with anyone (other than government or law enforcement authorities or others if required by law) without your consent. You can find out more information regarding data protection by reading Syngene’s privacy policy for more information

I consent to include my information in Syngene’s clinical trial volunteer database

I confirm that I am an Indian resident

I confirm I am 18 years or above

Please read the FAQs to know more.

What is a clinical trial?

A clinical trial is a research study conducted on humans to answer specific questions about new treatments, vaccines, surgical procedures, or diagnostic procedures.

Here, the clinical study refers to understanding the absorption and effect of the drug on the body, as well as its safety and tolerability. The new drug developed by the sponsor is tested on humans along with an existing drug already on the market. A clinical trial is also performed to determine whether a new drug or device is safe and effective for people to use.

Syngene conducts clinical trials per international and national regulatory guidelines, ICMR- national ethical guidelines for biomedical and health research involving human participants, and new drugs and clinical trials rules of the Central Drugs Standard Control Organization (CDSCO). Moreover, each clinical study is reviewed and approved by an independent ethics committee whose primary responsibility is ensuring the trial participants’ safety and well-being.

What is the requirement?

You should be a healthy male /female who is more than 18 years of age and an Indian citizen.

What is involved?

You will be registered as a volunteer in our volunteer database. The clinical trial details and procedures involved in screening and enrolment will be explained to you. You will be required to sign an informed consent form before the start of any activity. You will also need to give your blood and urine samples, undergo ECG recording and physical examination by a doctor.

What are the risks?

Our medical team, comprising several doctors and staff nurses, will monitor your safety throughout your participation in the clinical study. You will undergo periodic checks by doctors and staff nurses to ensure your safety.

An adequate gap (washout period) is maintained between studies to ensure the washout of the study drug.

What are the side effects?

The side effects associated with the drug will be detailed out in the informed consent form. Common side effects are nausea, vomiting, and headache.

What is the informed consent document process?

It is a process where a volunteer is given a document containing detailed information about the following:

Purpose of the study
Procedures and treatment involved in the study, including study schedule
Inclusion and exclusion criteria
Study design, study drug
Potential risks and benefits
Confidentiality
Your rights as a participant

After you have read or heard the details in the informed consent form from the healthcare provider and clarified all your doubts, you are required to give your consent by signing the informed consent document.

Please note that you are free to withdraw your consent at any time for any reason.