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Phase I Clinical Trials
Phase II–IV Clinical Trials
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  Highlights

What’s New

 
Phase II–IV Clinical Trials

 

To maximize the value of the service we provide to our clients, we strive to involve ourselves early in the trial process. Our attention to and understanding of protocol requirements, participation in protocol design, national and international logistics support, strategic locations and our close relationships with investigator sites – developed even before the trial commences – all contribute to the added value we offer our sponsor clients.

Our meticulous attention to sponsors’ protocol requirements ensures that we confidently meet protocol specifications within budget and on time. Our hands-on, proactive involvement at investigator sites enables us to prevent protocol non-compliance. We correct on-site errors promptly, resulting in improved investigator site performance.

Our specialized, project-dedicated team of medical consultants offers its collective expertise to the clinical researcher and can be expanded to include clinical chemists, toxicologists, microbiologists, virologists, pathologists, dermatopathologists or haematopathologists depending on the project.

Our support of investigator sites includes the handling, dispatch and training required to meet the International Air Transport Association and ground transportation legislative requirements for dangerous goods and infectious specimens.

Situated just 15 minutes from Pearson International Airport, our main central laboratory is conveniently located to better serve our clients. Our centralized facilities also offer our clients the benefits of optimized resources and, ultimately, cost savings, while our strong partnership with LabCorp expands our capacity for global trials.



 
 
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