Established & Proven

More than 24-years of deep clinical research management experience

Avance Clinical is the largest specialist Australian CRO delivering quality clinical trials in Australia and New Zealand for international biotechs.

The CRO has been delivering clinical drug development services for international biotechs for FDA and EMA regulatory approval, for the past 24 years.

Early Phase

Avance Clinical focuses on servicing biotech clients in their early phases of drug development delivering fast, nimble, and adaptive client-oriented solutions.

Fast, nimble, and adaptive solutions

Avance Clinical focuses on servicing biotech clients in their early phases of drug development delivering fast, nimble, and adaptive client-oriented solutions.

Avance Clinical delivers customised solutions designed around specific client needs rather than a one size fits all approach.

Clinical Monitoring Management

All Avance Clinical trials are monitored in accordance with Australian and New Zealand regulatory requirements and ICH GCP.

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ClinicReady - get into clinic faster

With ClinicReady, Avance Clinical’s team can act as a surrogate drug development department for start-up companies.

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Data Management

Avance Clinical data management team have gained a world-class reputation for accuracy, precision, and quality of their biostatistics and pharmacokinetic (PK) analysis.

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eclinical

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.

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Project Management

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.

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Quality Assurance

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.

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Safety and Pharmacovigilance

Clinical trials safety monitoring and reporting is vital to ensure participant safety, data integrity and regulatory compliance.

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Medical Writing

The Avance Clinical biostatistics and pharmacokinetics experts provide specialist guidance for your clinical research trial design and analysis.

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Full Service CRO

Avance Clinical is the leading full-service CRO for international biotechs conducting early Phase clinical trials.

The latest technology for data compliance

The company has focussed on state-of-the-art technology and systems across all functional areas to provide clients with the most effective processes. Medidata, Oracle, and Medrio are just some of the technology partners.

Avance Clinical offers globally accepted data from an established clinical trial ecosystem, that includes world-class PIs and Sites that are able to rapidly access specialized patient groups.

The Australian Government R&D grant means up to 43.5% rebate on clinical trial spend
Site Initiation Visit (SIV) and Study Start can be achieved in 5 – 6 weeks
Globally accepted data
No IND required for clinical trials

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More benefits

Avance Clinical can leverage all the benefits of Australia and New Zealand’s clinical ecosystem to deliver your study

Almost half clinical costs

The Government R&D grant means up to 43.5% rebate on clinical trial spend

Rapid Start-up

Site Initiation Visit (SIV) and Study Start can be achieved in 5 – 6 weeks

Start-up time

Site Initiation Visit (SIV) and Study Start can be achieved in 5 – 6 weeks

No IND

No IND required for clinical trials

GMP material

Full GMP material is not mandated for Phase I clinical trials

Gene-therapy accreditation

Avance Clinical is an accredited gene-therapy CRO

Seasonal studies

Northern hemisphere Sponsors can conduct their studies year-round by taking advantage of Australia and New Zealand's counter-flu and allergy seasons

FDA and global regulatory data compliance

Major hospitals with world-class infrastructures and dedicated Clinical Trial Units with a long track record in FDA compliant research

Rebate

The Government R&D grant means up to 43.5% rebate on clinical trial spend

Start-up time

Site Initiation Visit (SIV) and Study Start achieved in 5 – 6 weeks

Capabilities

Full service CRO in Australia and New Zealand

An Experienced Team

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195
Studies in the past 5 years
150
Experienced Team Members
10,000
Participants past 5 years
24
Years of of CRO experience

“Avance Clinical’s clients are international biotech companies primarily from the United States, United Kingdom, Japan, China, South Korea, Taiwan, France, and Germany. These clients are seeking a premium CRO with the same experience and advanced technology platforms offered by the major global CROs, but with an agile and customer focused approach to clinical management in Australia and New Zealand.”

Supriya Lala KunduBest Practices Research Analyst, Frost & Sullivan

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