Site selection and investigator networks
Access to investigator sites and networks matched to your therapeutic area and timeline.
Clinical trial start-up in South Africa, activated cleanly
Study start-up is where African trials stall. Veltrion coordinates regulatory, ethics, sites and investigators into one activation plan, so your study opens on time and runs with a local counterpart accountable for delivery.
Sites, ethics, regulator and sponsor, coordinated through one accountable counterpart, not four disconnected vendors.
What study start-up with Veltrion covers
SAHPRA and ethics submissions
Coordinated regulatory and ethics submissions so approvals do not become the bottleneck.
Study start-up and activation
The full activation path from feasibility to first-patient-in, managed on milestones.
CRO and vendor coordination
We coordinate the CRO and specialist vendors so the sponsor has one point of accountability.
Common questions
Do you run the trial or coordinate it?
We coordinate and activate, providing the accountable local counterpart that aligns the CRO, sites, ethics and regulator. Specialist delivery is delivered through our network.
Which countries can you activate in?
South Africa is the anchor, with activation extending across East and West African markets through our regulatory and site networks.
How do you select sites?
By therapeutic fit, recruitment capability, regulatory standing and track record, not by convenience.
Tell us the market and the date.
Most of these resolve in one call. If there is no route worth taking, we say so on the call.