eClinical

The latest technology from industry leaders like Medrio and Medidata

The Avance Clinical team works with eClinical leaders such as Medrio, Medidata and Oracle to offer regulatory compliant and patient-centric tools for rapid start-up and continual data flow. Avance Clinical delivers I\improve patient engagement and data collection and ensures Sponsors can stay informed at every step with Sponsor visible portals.

eClinical Solutions

At Avance Clinical you have the option to deploy the latest eClinical solutions to maximise the value of your study data and deliver real-time visibility on study progress.

Former Medrio CEO, Mike Novotny, commented that “Medrio has supported numerous study starts in Australia, over 150 with Avance Clinical alone, and we’re always impressed with the speed of their timelines.”

eClinical Capabilities

Avance Clinical deploys the latest eClinical solutions including eSource, eConsent, and ePro to maximise the value of study data and deliver real-time visibility on study progress.

Clinical technology leaders

The team works with eClinical leaders such as Medrio to offer regulatory compliant and patient-centric tools for rapid start-up and continual data flow.

Avance Clinical’s eClinical solutions improve patient engagement and data collection and enable clients to stay informed at every step with ePortals.

The Avance Clinical Advantage

Avance Clinical delivers globally accepted data
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

eSource

  • Electronic consent including patient sign-off and investigator confirmation
  • Customisable to include animations, videos and questions as required
  • Forms customised by Avance Clinical Data Management team
  • Link via email to patient
  • Compatible with any device and internet system (smartphones, tablet, laptop, desktop)
  • Integrated with Medrio EDC
  • Link can be shared with HREC as part of submission package

eConsent

  • Direct data capture of source data on site
  • Forms customised by Avance Clinical Data Management team
  • Edit checks built into forms; instant firing of queries once data is entered
  • Option for data to be collected off-line and synced when on-line is available
  • Fully integrated with Medrio EDC, data visible for Sponsor review instantly
  • Remote monitoring and data review on ongoing basis
  • Avance Clinical provision of tablets if required

ePro

  • Electronic capture of patient-reported outcome, including diary data, dosing compliance, questionnaires, VAS/Pain scales
  • Forms customised by Avance Clinical Data Management team
  • Link via email to patient
  • Options for emails and reminders at set times during the day or week
  • Timezone adjusted to patient’s location
  • Compatible with any device and internet system (smartphones, tablet, laptop, desktop)
  • Fully integrated with Medrio EDC, data visible for Sponsor review instantly
eClinical Solutions

Learn more about how we work

Request a Proposal or Talk to our Team  CONTACT US

More benefits

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

Ready to Partner with Us?

Contact us