Our Services

Phase I–III Clinical Trials

End-to-end clinical trial services from feasibility through to submission. Nine specialist capabilities, one trusted partner.

Study Feasibility & Consultancy

Service / 01

Study Feasibility & Consultancy

Validate protocol, sites and timelines before you begin.

Our team brings deep expertise and hands-on hospital knowledge to every engagement.

We work as an extension of your team, providing senior-level input without the overhead of a large CRO.

Service / 02

Site Selection & Setup

Find the right sites and get them trial-ready, fast. Our experienced team delivers every project with the focus, flexibility and accountability that sponsors expect from a specialist CRO partner.

Site Selection & Setup
Protocol Design

Service / 03

Protocol Design

Scientifically robust, operationally feasible protocols.

Our team brings deep expertise and hands-on hospital knowledge to every engagement.

We work as an extension of your team, providing senior-level input without the overhead of a large CRO.

Service / 04

Regulatory Affairs

CTA, IND and CTIS submissions handled end-to-end. Our experienced team delivers every project with the focus, flexibility and accountability that sponsors expect from a specialist CRO partner.

Regulatory Affairs
Clinical Project Management

Service / 05

Clinical Project Management

Single accountable owner for delivery.

Our team brings deep expertise and hands-on hospital knowledge to every engagement.

We work as an extension of your team, providing senior-level input without the overhead of a large CRO.

Service / 06

Study Monitoring

Risk-based monitoring by experienced CRAs. Our experienced team delivers every project with the focus, flexibility and accountability that sponsors expect from a specialist CRO partner.

Study Monitoring
Biometrics

Service / 07

Biometrics

Data management, biostatistics and CDISC programming.

Our team brings deep expertise and hands-on hospital knowledge to every engagement.

We work as an extension of your team, providing senior-level input without the overhead of a large CRO.

Service / 08

Pharmacovigilance

ICSR processing, SUSAR reporting and QPPV services. Our experienced team delivers every project with the focus, flexibility and accountability that sponsors expect from a specialist CRO partner.

Pharmacovigilance
Medical Monitoring

Service / 09

Medical Monitoring

24/7 physician oversight and safety assessment.

Our team brings deep expertise and hands-on hospital knowledge to every engagement.

We work as an extension of your team, providing senior-level input without the overhead of a large CRO.