Clinical development solutions for biotech innovators

 

Proud to be the go-to CRO for biotechs dedicated to moving innovation to maximum patient impact.

Biotech-tailored, dedicated teams

From early-stage strategy development to trial execution and regulatory approval, the team we assemble for you will deliver the trial with speed, quality and flexible solutions.

Built on 25 years of unmatched experience supporting, scaling and launching innovation, our biotech-tailored process and dedicated teams emphasize adaptability and provide a structure for fast decision-making.

Clinical solutions and services

  • Trial design and planning
  • Novel and adaptive designs
  • Decentralized or hybrid clinical trials
  • Protocol validation and optimization
  • Feasibility
  • Investigator, site ID and site selection
  • Local start-up teams
  • Global project management
  • Clinical monitoring (CRAs, CTMs and centralized monitoring)
  • Investigator and staff training
  • Regulatory affairs and consulting
  • Country CTA submissions
  • Annual reporting
  • Data management
  • Biostatistics
  • Safety and pharmacovigilance
  • Data Safety Monitoring Boards (DSMBs)
  • Steering committees & clinical advisory boards
  • Medical monitoring and medical data review
  • Medical writing
  • Quality assurance
  • Marketing approvals

Drug discovery and development laboratory services

Flexibility for our biotech customers is critical, and this includes customized laboratory services. Our global laboratory services provider, IQVIA Laboratories, has a team of experts and a proven model developed to ensure superior delivery.

Your partner from clinical to commercial

From pre-clinical asset strategy and consulting to clinical trial design and execution, to market launch and commercialization — IQVIA Asset Maximizer provides a comprehensive suite of solutions to help your breakthrough get to patients, faster. Your dedicated IQVIA Biotech team will manage the entire clinical trial process, from design and strategy to execution.
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