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Our Full-Service Clinical Research Units

Quebec City, Canada

Celebrating more than 30 years of excellence in early phase research

First established in 1994, today this is a 25,000 sq. ft. state-of-the-art facility, with up to 202 beds in five independent units as well as a full-service Bioanalysis laboratory, staffed by approximately 160 on-site nurses, pharmacists, clinical research associates and biometricians. The facility is equipped to conduct complex, high-intensity clinical studies with participant comfort and safety top of mind.

Key features include:

  • Wide range of healthy participant and patient enrollment capabilities that seek to meet the specific needs of your study
  • On-site pharmacy (temperature and humidity-controlled) equipped to perform nonsterile compounding and aseptic preparations (clean room)
  • Extensive participant data base and access to special populations
  • Two screening centers: Quebec City, with a satellite center in Montreal
  • Five km from hospitals with emergency facilities
  • Recognized and frequently inspected by worldwide regulatory agencies, with a strong reputation for safety and compliance, with no 483s on last five FDA inspections
  • On-site deployment of the ClinSpark® eSource platform, offering e-data capture and management specifically designed for Phase I clinical trials

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An unwavering commitment to safe and ethical early phase research

Our first concern is participant welfare as we strive – in partnership with our customers – to advance the delivery of life-changing therapies.

In addition to being subject to multiple layers of external oversight, Syneos Health has its own robust internal controls and processes to address participant safety and well-being, including:

  • A thorough informed consent process that clearly describes study requirements, risks and the need for participant transparency
  • Rigorous medical screening to determine study eligibility
  • Around-the-clock monitoring to promptly address potential adverse events

These activities are subject to Sponsor audit or Health Authority inspection.

Our additional full-service clinical research unit is located in Miami, Florida, US

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