Avance’s Clinical Research Associates are fully trained to appreciate the complexity of each specific clinical research trial and ensure that monitoring is conducted to the highest standard.
All trials are monitored in accordance with Australian regulatory requirements and ICH GCP. To ensure the seamless exchange of information each clinical research trial is assigned a Project Manager as a single point of contact.
Avance has staff experienced across all phases of clinical trials and collaboratively supports the Australian CRO arm of multinational trials.
- Avance’s Quality Assurance department audits and reports on the monitoring, collection and reporting of accurate, precise, and valid data.
- Avance has an extensive Suite of Standard operating procedures to conduct clinical research trial activities. Additionally, Avance can adapt seamlessly to your SOP and requirements if desired.