How ClinicReady delivers foundations for success
ClinicReady is the surrogate or outsourced drug development team for preclinical biotechs.
The ClinicReady scientific and regulatory affairs process supports demonstration of safety and preliminary clinical Proof of Concept (POC) and lays the vital clinical foundations that ensures seamless transition into phase two and beyond.
ClinicReady is designed for start-up companies who are looking to benefit from an outsourcing model of drug development execution.
get in touch with our
clinical operations team
Delivering more than 30 years experience of drug development expertise
In-house Scientific
and Regulatory Affairs Team
ClinicReady is the in-house scientific and regulatory affairs expert team, your surrogate drug development team.
The ClinicReady process supports demonstration of safety and preliminary clinical Proof of Concept and lays the vital clinical foundations that ensures seamless transition into phase one and beyond.
ClinicReady Success Story
Tetherex Pharmaceuticals
"The Avance team demonstrated flexibility and a solution-oriented attitude in working with us towards obtaining rapid ethics approval, thereby facilitating trial initiation in a timely and efficient manner." - Dr. Russell Rother, President and Chief Operating Officer
WHY BIOTECHS CHOOSE
AVANCE CLINICAL
More than three decades of deep clinical research management experience, Avance Clinical is the largest
specialist Australian and US CRO delivering quality clinical trials in Australia, New Zealand, Asia and North America for international biotechs.
43.5%
REBATE
5-6 Wks
START-UP TIME
100%
CAPABILITIES
FDA
COMPLIANT RESEARCH