Start-up you can plan around
A start-up tracker per site covering contracts, EC submission, training and SIV readiness, shared weekly.
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For sponsors and CROsA site partner that procurement and clinical operations can both trust
We work as an extension of your study team: transparent scope, documented processes and status reporting you don’t have to chase.
Visible enrolment
Weekly screening, enrolment and retention figures per site, with early flags when a site is behind plan.
Inspection-ready conduct
Work runs on written SOPs aligned to ICH-GCP E6(R3) and NDCT Rules 2019, with training records for every staff member.
Clear commercial terms
Unit-based or FTE-based pricing, itemised by activity, agreed before work starts. No hidden pass-through fees.
Data protection
Participant data handled under documented DPDP Act controls, with role-based access and confidentiality agreements.
Singapore coordination
A Singapore liaison for regional sponsors and CROs managing India sites alongside APAC programmes.
Engagement models
Choose how you work with us
| Model | Best for | What’s included |
|---|---|---|
| Full site management | Sponsors and CROs who want a turnkey India site network | Feasibility, start-up, CRC staffing, IP support, data entry, monitoring support and close-out |
| CRC staffing | Studies with sites that already have strong investigators but no coordinators | Trained coordinators, supervision, back-up cover and performance reporting |
| Start-up only | Tight activation timelines | Feasibility, contract and EC coordination, ISF set-up and SIV readiness |
| Rescue support | Sites behind on enrolment or data | Recruitment review, data backlog clearance and query closure |
Vendor qualification
Ready for your vendor assessment
We expect to be qualified before we are contracted. On request we share our SOP index, training matrix, organisation chart, data protection approach and insurance details, and we welcome qualification audits.
Typical documents available for qualification
- SOP index and sample SOPs
- Staff CVs, GCP training certificates and job descriptions
- Data protection and confidentiality policy
- Quality management and CAPA process description
- [Insurance certificate: to be added]
Start a conversation
Planning a study in India?
Share your protocol synopsis and target indication. We will come back with a site feasibility view within five working days.