Our Medical Writing and Clinical Trial Support Services
Stridon Clinical Research is a CRO specialising in Medical Writing and Regulatory support for clinical trials. We help our pharma and biotech clients get regulatory approvals, with no hassle and at the first attempt, by producing expertly written clinical trial and regulatory documentation. This includes high quality clinical trial protocols, study reports, investigator’s brochures, and IMPDs.
Our service portfolio also includes training for clinical trial staff, GCP and GMP audits, and clinical trial site management.
Led by its founder Dr Radivoj Arezina, Stridon provides Medical Writing and the associated services to its clients in the UK and internationally.
Why Choose Us
We pride ourselves on delivering high quality clinical trial support services, reliably and on time. Our expertise is underpinned by many years of first‐hand experience in clinical trial design, conduct, regulatory oversight and reporting. Our approach is to provide tailor‐made service with an ethos of treating every client special regardless of their size.
Get in touch
Contact us now to receive more information about the services we offer to clinical research establishments