Medical Device & Diagnostics

Pave your path to market

With experience in most device types, Quintiles optimizes development processes and regulatory pathways to help bring new medical devices and diagnostics to market quickly – and keep them there for commercial success.

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Named to InformationWeek Top 500 list of Information Technology Innovators

Quintiles was named to InformationWeek Top 500 list of Information Technology Innovators for five consecutive years.

Equip your product for success

Helping your device or diagnostic realize its full potential requires navigating complex regulatory and development environments.

Extensive experience for comprehensive insights

Our medical devices and diagnostics services span the globe (including United States, Europe, Latin America and Asia Pacific) and include:
  • Preclinical and regulatory consulting 
  • Clinical trial services
  • Post-market interventional studies
  • Post-market observational studies
  • Our expert team includes industry veterans and ex-agency personnel who draw from their experience in the US Food and Drug Administration (FDA), the FDA's Center for Devices and Radiological Health (CDRH) and almost every device review organization within the FDA. 
We also bring you the dedicated expertise of Novella Clinical, a Quintiles Company, which offers more than a decade of experience and a broad range of therapeutic concentrations in devices and diagnostics, including cardiovascular, orthopedic/spine, general surgery and oncology.

The power of possibilities

With Quintiles, you have the regulatory expertise and global footprint to support your medical device success.

Related services

Real-world research to determine real-world impact
Respond to changing markets with experienced, agile sales teams
A proven approach to achieving commercial success
Quintiles Recent Awards