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Clinical Trials

In conjunction with specialist CRA/CRO consultants, we can assist you with:

  • Developing a tailored Clinical trial strategy for your company's product(s). 
  • Applying Good Clinical Practice (GCP) principles to your clinical trial. 
  • Incorporating health economic data collection into your clinical trials so that you can save time in obtaining 
    reimbursement for your product. 
  • Designing and managing clinical trials. 
  • Writing submissions to ethics committees and regulatory authorities to conduct clinical trials in Australia, 
    the EU, the US and Canada . 
  • Writing documents for clinical trials such as clinical trial protocols, investigator brochures, CRF's, clinical 
    trial reports, etc. 
  • Liaison with ethics committees and regulatory authorities.