With our exceptional depth of knowledge in medical devices, novel technologies, and combination products, only Avania has the focus and experience you need.

Conducting a clinical trial is overwhelming; meeting critical milestones, managing your budget, and speeding your product to market. With Avania, you’re partnered with a project manager who drives the entire trial execution team. With their effective leadership skills and industry expertise, our project managers excel in the oversight of trial conduct, progress reporting, risk mitigation, and budgeting. Our project managers are adept at providing excellent client service and proactive communication.

An understanding of the given therapeutic area is central to our project managers’ success, so we assign them based on therapeutic expertise. They work on first-in-human, feasibility, pivotal, and post-market trials across the globe. All project management activities are conducted in compliance with the trial’s protocol, project plans, standard operating procedures, ICH GCP, ISO 14155, and all applicable regulations and guidelines.

Let us help you while you’re developing your product.

  • Clinical operations team that works collaboratively with investigators and sponsors, reinforcing patient safety, trial data integrity, and protocol compliance

  • 30+ years of therapeutic and surgical expertise
  • In-person technical training for investigators
  • Collaborative relationships with sites and investigators for seamless execution

  • Oversight of trial team member activities
  • Creation of project management plans
  • Management of timelines and deliverables
  • Budget tracking and management of quality deliverables
  • Proactive communication with the sponsor, vendors, and sites
  • Management of predefined metrics and study trends
  • Oversight of data quality

  • Pilot and early feasibility, emphasizing learning and flexibility, first-in-human
  • Pivotal and registrational, emphasizing efficacy and effectiveness
  • Quality of life and health economic outcomes, emphasizing patient impact
  • Postmarket and registries, emphasizing market intelligence
  • Distributor searches in Australia and New Zealand
  • Field support
  • Medical affairs
  • Medical writing, including clinical evaluation reports
  • Quality management
  • Regulatory affairs
  • Reimbursement programs