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QAReady - QA Consulting Service

Data quality is at the heart of everything

QAReady provides independent Quality Assurance services

Data quality is at the heart of everything at Avance Clinical. Delivered by our highly experienced staff we support our clients with designing their clinical trial audit strategy to provide assurance that their study meets GCP requirements.

Vast Experience

Our independent Quality Assurance team provides a full range of independent Quality Assurance services. Our auditors have vast experience in conducting clinical trial audits in various phases and therapeutic indications, across several regions including APAC, EU, and USA.

Creating Audit Plans, Selection of sites for audits
Investigator’s Site Audits
Vendor Qualifications and Vendor Audits
TMF Audits
Clinical Study Report Audits
QA Consulting

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QAReady

Learn more about our services

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
No IND required for clinical trials
Globally accepted data

Request a Proposal or Talk to our Team  CONTACT US

More benefits

Avance Clinical can leverage all the benefits of Australia, New Zealand and North America’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

QAReady – data is everything. Talk to us today.

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