How to speed up site start-up by 50%: Part 2 – Contract Negotiation
Like patient consent forms, site Clinical Trial Agreements (CTA) have become increasingly complex, making their review a major roadblock to…
How to speed up site start-up by 50% Step 1: Reverse Feasibility Approach
Data from the Journal of Clinical Oncology suggests that the average U.S. site start-up time is approximately 36 weeks**. In…
Why Canada is well suited for YOUR oncology clinical trials
To make it to the winner’s circle in this industry, you must know your strengths and leverage them to maximize…
Quality, Speed & Performance – Keys to Canada’s Future – Interview with Karen Arts of the Ontario Institute for Cancer Research
Canada boasts several centers of excellence with a group of internationally renowned investigators that are at the forefront of oncology…
Value of Canadian Oncology Centers for Early Phase Trials – Interview with Dr. Stephen Welch
Given the increased focus on speed of activation for oncology studies, sponsors are under pressure to select top-performing investigative sites…
Patients are the KEY Stakeholders in Clinical Trials
Last week I had the pleasure of sitting down for lunch with Sandra Gazel (@sgazel). Sandra is one the most…