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“We aim to give clients unparalleled service to optimise the timely and cost effective completion of projects. It’s as simple as that”.

- Yvonne Lungershausen -

Conducted to the highest ethical and regulatory standards, and employing stringent Quality Assurance procedures, CPR customises its approach to meet the specific objectives of each and every client.

CPR has extensive experience in the project management, monitoring, data management, and statistical services of Phase I studies, with our expertise extending across Phase II & III.

As the only Australian CRO that can provide all services in-house, CPR's synergistic combination of clinical and data management services with GLP accredited bioanalytical laboratories ensures projects are delivered on time and on budget.

Led by Yvonne Lungershausen, CPR's Clinical Specialists can assist with:
  • Phase I-III trials
  • Bioequivalence studies
  • Bioavailability studies
  • Clinical pharmacokinetics
  • All therapeutic areas
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