Ethics Committee Coordination
Document readiness, submissions & responses in coordination with sponsor/CRO.
CTM
Clinical Trial Management Support
Program coordination from feasibility through closeout under client SOPs.
Related support services
Regulatory Affairs Support
Dossier preparation, trackers & clarifications; filings done by sponsor/CRO or by us when authorized.
Pharmacovigilance Support
ICSR intake/processing, E2B checks, QC & medical review support per client safety SOPs.
Need Trial Management Support?
Tell us about your programme and we’ll come back with a work plan covering scope, governance and timelines.