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How ClinicReady Delivers Foundations For Success

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ClinicReady is the surrogate for outsourced drug development team for preclinical biotechs.

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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.

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.

Scientific & Regulatory Affairs

The ClinicReady team of scientific and medical affairs specialists consists of PhD-qualified professionals with three decades of industry and academic research experience.

  • Regulatory agency submission support

    • Designed from the start for approval

  • Trial Design

    • POC and key data collection

  • Protocol Review

    • Experienced medical and scientific team

  • Incorporating Later Phase Strategy

    • Drug development roadmap for success

Surrogate Drug Development Team

Our team of scientific and medical affairs specialists provides proactive guidance to clients at the early stages of development, before they embark on preclinical safety and toxicology activities. This ensures that they undertake a the right preclinical studies, enabling them to gather the necessary data for the approval of their first-in-human study.

  • Gap Analysis

    • Data analysis for accurate planning

  • Preparation of Drug Development Plans

    • Drug development journey planning

  • Pre-clinical vendor selection and management

    • Trusted and proven vendor partners

  • Scientific Advice

    • PhD-qualified professionals with three decades of experience

Clinical trial designs

The experienced team provides clients with a comprehensive raft of scientific, regulatory, and Medical writing services, including preparation of investigator’s brochures, clinical trial designs, study protocols, and patient information and consent forms as well as clinical trial data and clinical study reports.

  • Therapeutic Area Advice

    • Tapping three decades of experience

  • Chemistry Manufacturing Controls (CMC) Advice

    • Specialists for advice at every stage

  • Preparation of Investigator’s Brochure

    • Expert communication of study design and process

  • Medical writing services

    • Integrated into ClinicReady for streamlines production

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

Avance Clinical