We have expanded to the US
With the acquisition of US-based CRO C3 Research,
Avance Clinical now offers its international biotech clients
CRO services in Australia, New Zealand, and North America
Globally accepted data
Avance Clinical has a world-class reputation for quality data that is accepted by all regulatory authorities including FDA. In-house Medidata trained specialists.
Avance Clinical can deliver Site Initiation Visit (SIV) and Study Start in 5 – 6 weeks. No IND required.
Extend budget by 43.5%
Avance Clinical can secure the maximum rebate on your clinical trial spend with the Australian Government clinical trial rebate program.
Avance Clinical invests heavily in the industry-leading technology platforms to support speed, communications, and regulatory compliance.
Established & Proven over 24 years
Agile and solutions-focussed
More than 200 In-House CRO Specialists
The ClinicReady range of services constitutes a natural progression in Avance Clinical’s role as the premier provider of early drug development support to the biotechnology sector. The company recognises the major challenges faced by small biotechnology companies, particularly start-up companies who seek to drive their novel therapeutics to demonstration of safety and preliminary clinical Proof of Concept.
Safety and Pharmacovigilance
Clinical trials safety monitoring and reporting is vital to ensure participant safety, data integrity, and regulatory compliance.
Regulatory guidelines around clinical trial safety monitoring and reporting demand strict safety management procedures, from a highly-skilled, and experienced safety team.Discover More
The Avance Clinical team works with eClinical leaders such as Medrio, Medidata, and Oracle to offer regulatory compliant and patient-centric tools for rapid start-up and continual data flow.Discover More
Data quality is at the heart of everything at Avance Clinical. Delivered by our highly experienced staff we support our clients with their clinical trial audit to achieve their quality objectives for their clinical research trials.Discover More
Clinical Monitoring Management
Avance Clinical has experienced clinical monitoring staff across all phases of clinical trials and can collaboratively support the Australian CRO arm of multinational trials.Discover More
Avance Clinical provides each clinical research trial with a dedicated Project Manager to ensure that milestones are reached, timelines are met and that our clients receive effective communication and ongoing status reports.Discover More
“It has been a great pleasure working with you on this project. Your flexibility, pragmatic approaches and focus on the work has been exceptional. I am looking forward to have the next compound entering the clinic with you.”Head of Drug Discovery, Pharmaxis Ltd
“Working with the Avance Team has helped us to develop and complete high quality and compliant clinical studies. I especially appreciate their penchant for communication, quality and pragmatism.”Sr. Vice President, Regulatory, Quality & Clinical Affairs, Atossa Genetics, Inc.
“Having conducted several Phase I studies in Australia it made sense to continue in the country with our Phase II program, particularly given the high-quality support we have received from our CRO.”Atossa Therapeutics Inc.
“Avance Clinical has proven themselves to be my “Champions”, anticipating problems and always acting in the interest of getting the trial done professionally, resourcefully, and in alignment with the goals of the Sponsor and well-being of the volunteers.”Chairman of the Board and Chief Medical Officer, BioFactura Inc
“Medrio has supported numerous study starts in Australia, over 150 with Avance Clinical alone, and we’re always impressed with the speed of their timelines.”CEO Mike Novotny (former), Medrio
“We reached out to Avance to refine and polish a substantive and comprehensive drug study clinical trial ethics application. The Avance Team were remarkably quick to respond to our enquiry. Avance provided us within a very short turn-around period a comprehensive appraisal of the documentation covering all elements including protocol, ethics, investigator brochure and patient information and consent. Avance were highly engaged with the research investigator team and suggested changes were clear and well rationalised. The services provided were cost-effective and well justified. I have no hesitation to recommend Avance as a quality CRO”.Curtin Health Innovation Research Institute
View our latest client and company