Make a Difference

Become a Clinical Study Volunteer

Clinical research only moves forward because of the courageous individuals who volunteer to participate in studies. As a volunteer at Lazent Clinical, you are contributing to the development of medicines that will benefit patients around the world.

Why Volunteer

Your Role Matters

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Your Contribution Matters

Your participation helps scientists understand how medicines work in the human body — accelerating the development of safer, more effective treatments for patients globally.

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You Are in Safe Hands

All studies are conducted under strict GCP guidelines with 24/7 medical supervision, fully equipped ICU-level emergency facilities, and independent ethics committee oversight.

Clinical Trial Volunteers
Who Can Volunteer

Eligibility Criteria

General eligibility criteria for healthy volunteer BA/BE studies:

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Age: 18–45 years (may vary by study protocol)

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Gender: Male or Female — as specified per study requirements

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BMI: 18.5–29.9 kg/m² (healthy weight range)

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Non-smoker or ex-smoker (must have quit >1 year prior)

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No history of significant medical conditions (cardiac, hepatic, renal, neurological, etc.)

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Not currently taking any prescription or non-prescription medications

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Not pregnant or breastfeeding (for female volunteers)

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Willing to stay at the facility for the required confinement duration

Note: Final eligibility is determined at medical screening. All inclusion/exclusion criteria are study-specific and confirmed at enrollment.

The Process

How It Works — Step by Step

1

Register Your Interest

Complete the online registration form or call our volunteer helpline. Our coordinator will contact you within 48 hours.

2

Pre-Screening Call

A brief telephonic pre-screen to check basic eligibility criteria before you visit the facility.

3

Medical Screening Visit

A detailed medical examination including physical check-up, lab tests (blood, urine), ECG, and vital signs assessment — all at no cost to you.

4

Study Enrollment

If you meet all eligibility criteria, you will be enrolled into the study and given a full briefing on what to expect.

5

Informed Consent

A qualified clinician will explain the entire study in your preferred language. You are free to ask any questions before signing consent.

6

Check-In & Confinement

Arrive at our facility for the study period. You will be housed, fed, and monitored by our clinical team throughout your stay.

7

Study Completion & Follow-Up

After the study, you will receive a medical follow-up and your participation compensation will be processed.

Questions?

Volunteer FAQs

Yes. All studies conducted at Lazent Clinical are reviewed and approved by an Independent Ethics Committee (IEC), conducted under GCP guidelines, and supervised by qualified medical personnel 24/7. Emergency facilities including ICU-level care are on-site at all times.
Yes. Volunteers receive compensation for their time, travel, and inconvenience. The amount is determined per study protocol and is fully disclosed before you give consent.
Absolutely. Participation is entirely voluntary. You may withdraw from the study at any time without giving a reason and without any penalty or impact on your future eligibility.
Confinement duration varies by study — typically between 1 and 5 days for standard BA/BE studies. Long-housing studies may require longer stays. All durations are disclosed during consent.
You will have meals provided per the study protocol, access to a recreation area, and full access to clinical staff. Blood samples will be collected at scheduled timepoints per the protocol.

Ready to Make a Difference?

Register as a volunteer today and our coordinators will be in touch within 48 hours.

Register as a Volunteer →

Volunteer Helpline: +91-77956-44646 | Email: BD@lazentclinical.com