The Avance medical writing team offers high quality in-house CRO services, including protocols and reports.
Our biostatistics and pharmacokinetics experts provide guidance for your clinical research trial design and analysis. For both healthy volunteer and patient studies, Avance has strong co-existing relationships with all Phase 1 units across Australia as well as clinical sites and specialists in a variety of therapeutic areas.
The protocols our team prepare are developed in compliance with the Guideline for Good Clinical Practice ICH E6 (R2). Clinical Study Reports (CSRs) are prepared according to the Guideline for Structure and Content of Clinical Study Reports ICH E3 by our team of Medical Writers, in collaboration with our biostatisticians and pharmacokineticists.
- Investigator Brochures
- Clinical Study Reports to ICH E3
Contact us to talk to our highly experienced team regarding your next clinical research trial.