Our Services
What We Do
Our Expertise
Feasibility & Consultancy
Validate protocol, sites and timelines before you begin.
Protocol Design
Scientifically robust, operationally feasible protocols.
Regulatory Affairs
CTA, IND and CTIS submissions handled end-to-end.
Clinical Project Management
Single accountable owner for delivery.
Study Monitoring
Clinical monitoring by highly experienced CRAs.
Biometrics
Data management, biostatistics and CDISC programming.
Pharmacovigilance
ICSR processing, SUSAR reporting and QPPV services.
Medical Monitoring
24/7 physician oversight and safety assessment.