The Avance Clinical biostatistics and pharmacokinetics experts provide specialist guidance for your clinical research trial design and analysis.
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 for both healthy volunteer and patient studies.
The protocols prepared 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 in collaboration with the Avance Clinical biostatisticians and pharmacokineticists experts.