Australian Healthcare Solutions offers the full spectrum of CRO and technical support services required to seamlessly run your device trial in Australia and New Zealand geographies.

Our CRO services

Our CRO and technical support service offering is flexible. We can partner with you to fully manage your clinical trial from beginning to end or we can customise a suite of services to meet your specific trial needs:

  • Project management
  • Key Opinion Leader and site identification
  • Preparation Ethics (HREC) submissions and amendments
  • Management regulatory requirements
  • Site initiation and training
  • Trial master file development and management
  • Clinical field support
  • Sponsorship facilitation
  • Monitoring
  • Subject recruitment
  • Study close out

Medtech specialists
Australian Healthcare Solutions (AHS) specialises in running medical technology trials. We work with medtech companies at any stage of their commercial journey. We are equipped to run small single site, first-in-human trials through to multi-centre sites within Australia and New Zealand. Similarly we are positioned to run the Australian arm of multi-national trials.

We work with device technologies across a broad clinical spectrum with specific clinical expertise and relationships in Respiratory, Cardiology, Cardiothoracics and Interventional Radiology spheres.

Quality and efficiency
At AHS delivering quality is our priority. Our clinical research services are all built on and delivered according to Good Clinical Practice (GCP) principles and standards. Our team of project managers, monitors and clinical support staff all practice according to GCP standard.  They are experts in their fields with clinical experience matched to your technology.

At AHS we know that getting a technology to trial start up and ultimately to market as quickly as possible is a key goal. At AHS our understanding of the device trial landscape in Australia and New Zealand coupled with the strength and depth of our relationships with physicians and trial sites and our familiarity with local HREC requirements enable us to efficiently navigate and manage trial processes.