Services & Expertise

Services

Our core services include:

• Coordination of Phase I though IV Clinical Trials
• Pharmacokinetic, pharmacodynamic and biomarker studies
• Proof of concept trials
• Standardized protocols for adjuvant drug studies prior to radical prostatectomy (allowing tissue analysis following drug exposure)
• Safety/efficacy studies with single agent or combination therapies
• Long term surveillance studies
• QOL and outcome studies
• Development of clinical trial protocols
• Biomarker and assay development
• Preparation of regulatory and ethical documentation for submission to health Canada and Institutional Review Boards (IRBs)
• Negotiation of Clinical Trial Agreements and Budgets
• Development of study specific SOPs
• Collection, entry, processing and analysis of clinical trials data and patient derived samples
  • Experience with both paper and electronic CRFs
• Preparation of clinical study reports
• Access to national and international multi-centre networks for GU tumor clinical trials

Expertise

The Clinical Trials Service at PC-TRIADD builds on more than 20 years of experience in conducting superior quality clinical trials in a variety of indications. Our highly-qualified team of investigators and support staff include:

• Four full-time urologists
• Three full-time medical oncologists
• Nine full-time clinical trial coordinators
• Six registered nurses
• Three regulatory affairs assistants
• Administrative support staff