From site activation to close-out, Medwave handles clinical monitoring and site management across neuro-oncology and radiation oncology trials. We know these indications, the sites that run them, and what it takes to keep a study on track. We also support partner organisations with knowledge transfer for CRAs stepping into these indications for the first time.
Site Set-up & IRB Coordination
End-to-end site activation support, including site feasibility and selection, contract negotiations, ethics committee and IRB submissions, and regulatory documentation. Everything in place before the first patient arrives.
Neuro-oncology Monitoring
A dedicated group of CRAs with hands-on experience in neuro-oncology and radiation oncology, across both drug and device trials. They understand what these indications demand and how to monitor them accordingly.
CRA Training & Development
Hands-on knowledge transfer for CRAs from partner organisations working in neuro-oncology for the first time. We share practical know-how on PFS endpoints, RANO assessment criteria, pseudoprogression, and the day-to-day monitoring realities of GBM and other brain tumour trials, learnt from years on the ground in these studies.
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