Clinical Trials
Global Clinical Trial Network
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Find paid clinical trials and clinical studies near you.

See clear study details, check if it may suit you, and choose a screening time. We guide you one step at a time.

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Volunteers registered
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CROs registered
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Organisations registered
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What would you like to do?

I want to join a study

Find studies, see payment, and apply online.

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I run a study centre

Post studies and manage volunteer screening.

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I represent a sponsor

Find and compare trusted research partners.

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Built around your role

Understand what the platform does for you before you sign in.

For Volunteers

Find studies without feeling lost.

The current problem: Study information is often difficult to understand, forms are repeated, and people may not know what happens after applying.

Our solution: See simple study details, apply step by step, choose a screening time, and follow every update from one place.

How it helps: Spend less time repeating information, understand each decision, and stay in control of what you share.

View open studies
How it works
  1. 1Create your profile once
  2. 2Choose a suitable study
  3. 3Apply and book screening
  4. 4Track the result on your dashboard
Trust and security

Your identity and health details are private. A study team sees only information you explicitly allow for that study.

Role-specific access
For CROs

Recruit and screen volunteers with less manual work.

The current problem: Applications, eligibility checks, appointments, and waitlists are often spread across calls, messages, and spreadsheets.

Our solution: Publish studies, review applications, approve suitable volunteers, manage screening dates, and monitor waitlists in one work area.

How it helps: Fill studies faster, reduce missed follow-ups, and present verified capabilities to relevant sponsors.

Register your CRO
How it works
  1. 1Register your organisation
  2. 2Publish a study
  3. 3Review and approve applications
  4. 4Manage screening and waitlists
Trust and security

CRO teams see only their own studies and the volunteer information released for those studies. Access is recorded.

Role-specific access
For Sponsors

Choose research partners using relevant evidence.

The current problem: CRO selection can depend on referrals and scattered documents, making fair comparison and follow-up difficult.

Our solution: Define a trial project, match suitable CRO capabilities, compare partners, build a shortlist, and send structured briefs.

How it helps: Reduce partner-search time, improve fit, and keep proposals and decisions connected to each trial project.

Sponsor sign in
How it works
  1. 1Create a sponsor profile
  2. 2Define the trial need
  3. 3Compare and shortlist CROs
  4. 4Send briefs and track replies
Trust and security

The partner directory is private to authorised sponsor and administrator accounts. Sponsors never see volunteer health or identity data.

Role-specific access
Accepting volunteers now

Studies open near you

See the payment, location, and dates before you apply.

See all studies

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Match indications are advisory. Final eligibility is always decided by the study site at screening.

01
Portable volunteer identity
02
Connected product modules
04
Commercial relationships
100%
Consent-gated data access
The problem

Clinical research still runs on fragmented trust.

Every study rebuilds the same identity, consent and screening steps. Volunteers repeat KYC at each site, CROs cannot see cross-participation risk until it is too late, and sponsors choose research partners with little comparable data. Consent is often a one-time signature rather than a living permission, and audit trails are scattered across emails, spreadsheets and site files.

  • Repeated KYCVolunteers fill the same identity and health forms at every centre.
  • Blind spotsA CRO cannot see a volunteer’s recent participation at another site.
  • Opaque selectionSponsors compare CROs through referrals instead of structured capability data.
  • Static consentOnce signed, volunteers rarely control what is shared, for how long, or with whom.
The Clinical Study Passport solution

One portable identity. Clear boundaries. Verifiable trust.

Clinical Study Passport replaces repeated onboarding with a reusable Clinical Study Passport, replaces blanket consent with purpose-bound, time-limited permissions, and replaces opaque CRO selection with a structured global directory. Every access is logged, every role sees only what it needs, and source clinical records stay with the site that created them.

  • Portable passportOne verified identity and study-history ledger across participating networks.
  • Consent-gated accessVolunteers choose exactly what each CRO sees, and can revoke it at any time.
  • Cross-participation signalElapsed-days and dosing-block signals appear before screening, not after.
  • Trusted CRO directorySponsors compare, shortlist and brief research organizations in one place.
How it works

From passport to consent-gated access — then back again.

Clinical Study Passport closes the loop between volunteers and research centres. The volunteer builds one record, the CRO requests only what the study needs, and every update feeds back into the same trusted history.

Step 01

Tell us about yourself

Create your free profile once. Add your age, city, and basic health details so we can show studies that may suit you.

Step 02

Choose a study

Read the payment, dates, location, and requirements in simple language. Apply only when you feel ready.

Step 03

Book your screening

Pick a convenient time to visit the study centre. The medical team makes the final decision after your health check.

Create your passportVerify a passport QR
One network · Two products

Infrastructure for the full study journey.

Clinical research is global, but trust remains fragmented. Clinical Study Passport creates a shared operating layer without collapsing the boundaries between commercial selection, personal data and clinical source records.

Clinical Study Passport Discover

Find and evaluate CROs globally

Sponsors compare research organizations by geography, study phase, therapeutic experience, site capacity and regulatory track record, then send a structured trial brief directly to a shortlist.

Explore Discover →
Clinical Study Passport

Carry one trusted study identity

Volunteers control a reusable identity, eligibility profile and participation ledger. CROs recruit against clear rules while seeing only the data a volunteer has actively released.

Open Passport →
The Clinical Study Passport trust architecture

Global reach. Clear data boundaries.

01Partner discovery

A sponsor finds the right CRO

Discover turns CRO capabilities, geographies, therapeutic experience and regulatory history into a comparable global directory — without moving patient data.

02Consent-first recruitment

The CRO recruits the right volunteers

Passport matches against de-identified eligibility signals first. Identity and supporting information are released only after an explicit volunteer decision.

03Continuous trust

The record travels, ownership does not

Volunteers carry a portable history. CROs and sites retain the clinical records they originate. Every permitted access remains scoped, expiring and auditable.

Consent boundary

Who can see what — and why.

Clinical Study Passport is built on role-based access. Each party sees only the data required for its role, and nothing is visible without an explicit consent action.

Volunteer

Owns the passport. Sees full identity, documents, study history and every access log. No one else sees anything by default.

CRO / Site

Sees de-identified eligibility signals before consent. After consent, sees only the identity, documents and fields the volunteer released for that study window.

Sponsor

Browses the CRO directory and trial brief responses. Has no access to volunteer identity or health data.

Compliance / Admin

Audits subscriptions, consents and access logs. Does not browse clinical records or personal profiles by default.

Read the disclaimerPrivacy & data policy
Cross-participation transparency

Know how long it has been since a volunteer's last study.

Volunteers who move between research centres are invisible to any single CRO. Clinical Study Passport turns participation records contributed by participating organisations into one clear signal: the days elapsed since a volunteer's last recorded dosing or study exit — available before screening and at every subsequent period check.

  • Interval checkSee the elapsed-days signal on a volunteer before screening, not after.
  • Dosing blockMark a volunteer as dosed so other centres see the interval reset immediately.
  • Shared contributionThe signal is only as complete as the records participating organisations contribute — so contribution is part of access.
  • Consent boundaryInterval signals are de-identified. Identity and documents move only on an explicit volunteer decision.
Built for every participant

One platform, role-specific control.

01

Sponsors

Source and compare CROs across markets, issue trial briefs and track partner responses.

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CROs & sites

Publish capabilities, recruit eligible volunteers and manage access under explicit consent.

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Volunteers

Hold one portable identity, manage permissions and understand every access to personal data.

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Compliance teams

Review a clear ledger of consent, access and verification events without default access to all data.

Clinical Study Passport · Full V1

Eight modules. One continuous credential.

01

Volunteer onboarding & KYC

One verified identity and permanent CSP ID across participating research networks.

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Clinical Study Passport

A portable credential showing identity, status and participation history.

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Study discovery & matching

Transparent criterion-by-criterion matching with advisory washout checks.

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Consent-gated application

Every application raises a specific data-access request for the volunteer.

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Granular access control

Purpose-bound, time-limited and revocable sharing — nothing visible by default.

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Document wallet

Identity and medical documents shared only under explicit, expiring permission.

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Study history ledger

A continuous participation record while source clinical files remain with each site.

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QR verification

Short-lived verification tokens with every access written to the audit trail.

Questions & answers

What the passport shows — and what it does not.

Quick answers for volunteers and CROs about the Clinical Study Passport, consent boundaries and eligibility. Search below, or open the full FAQ.

For volunteers

What does my Clinical Study Passport show?▼

It shows your verified identity, contact and demographic details, your eligibility profile, uploaded documents you have chosen to share, and a ledger of your study participation history across participating organisations.

Open in full FAQ →
What does it NOT show or decide?▼

It never shows another volunteer's data, clinical source records held by a site, or any medical diagnosis. It also does not decide whether you can join a study — that is always the investigator's decision.

Open in full FAQ →
Who can see my passport?▼

By default, only you. A CRO or site sees identity, documents or eligibility details only after you explicitly consent to a specific application. You can review or revoke that access at any time.

Open in full FAQ →
Can I revoke access after I have granted it?▼

Yes. Every consent you grant is scoped, time-limited and revocable from your consent centre. Once revoked, the organisation loses access to the shared fields, and the revocation itself is recorded in your audit trail.

Open in full FAQ →
Can I remove my data?▼

Yes. You can request erasure of your passport data from within the app. We will delete your profile, documents, consents and participation records while keeping a minimal audit trail required by law.

Open in full FAQ →
Do I have to pay?▼

Creating a passport is free. Subscription plans (₹500 for 3 months, ₹1,000 for a year, ₹3,000 lifetime) unlock advanced visibility and sharing features. You choose whether to upgrade, and there are no usage-metered charges.

Open in full FAQ →

For CROs & sites

What can we see before a volunteer consents?▼

Only de-identified eligibility signals — for example, whether an anonymous profile matches your study's inclusion/exclusion criteria and the elapsed-days interval since their last recorded dosing.

Open in full FAQ →
What is shown after consent?▼

Once a volunteer approves your application request, you can see the identity, documents and profile fields they have explicitly shared for that purpose and time window. Every access is logged.

Open in full FAQ →
What is NOT in the passport?▼

The passport is not a medical record system. Source clinical records, pathology reports, imaging and investigator notes remain with the originating site. Clinical Study Passport only carries the participation ledger and what the volunteer chooses to share.

Open in full FAQ →
Does Clinical Study Passport guarantee eligibility or replace OVIS?▼

No. Matching and washout outputs are advisory inputs to your screening process. Final eligibility is determined by your investigator under your SOPs. Clinical Study Passport does not replace any national duplicate-participation registry.

Open in full FAQ →
How do we recruit through Clinical Study Passport?▼

Publish your studies, review anonymised matches, send consent-gated application requests, and track the funnel from view to enrolled — all inside the CRO dashboard.

Open in full FAQ →
What does CRO access cost?▼

Basic listing and match previews are free. Volunteer access and sponsor reach are each ₹5,000 for 3 months, ₹10,000 for a year or ₹30,000 lifetime. There are no per-unlock, per-brief or success fees.

Open in full FAQ →
What happens to our records if a volunteer erases their passport?▼

Their portable passport data is removed from Clinical Study Passport. Clinical source records you hold as the originator remain under your own retention obligations — erasure on Clinical Study Passport does not delete or alter your site records.

Open in full FAQ →
Browse the full FAQStill have questions?
Get started

Two clear next steps.

Choose the path that matches your role. Volunteers can create a passport in minutes; CRO and site staff can sign in to recruit or verify.

I am a volunteer

Create your free Clinical Study Passport, set your eligibility profile and control what each CRO can see.

Sign up as a volunteer

I am CRO / site staff

Sign in to recruit volunteers, review sponsor briefs, or verify a passport QR at a site checkpoint.

Sign in as CROVerify passport QR
Start with Clinical Study Passport

Build clinical research relationships on verifiable trust.

Browse the research partner network, create a portable volunteer passport or choose the subscription that fits your role.

For sponsorsBrowse open studiesView pricing