Do Data Entry Issues & Backlog Threaten Your Clinical Trial?
6 Critical Factors for Prevention & Mitigation Collecting clinical data that are accurate, reliable and of high quality is the…
What is Most Important When Conducting Oncology Clinical Research in Canada?
Developing oncology compounds is a constantly evolving process, and with the dramatic rise in costs, and competitive trials, making every…
How Do CRAs Proactively Manage Risk with These Soft Skills?
CRAs with Key Soft Skills Leads to Honest Communication and Better Risk Management at Sites Open communication with sites is…
What to Look for When Selecting a CRO – Real World Evidence
There is a myriad of factors involved in selecting a CRO. Do CRO team members have the necessary therapeutic expertise?…
2018 in Retrospect – Real World Evidence of Win-Win CRO/Sponsor Relationships
What’s in Store for 2019 and Beyond? The Clinical Trials Market was valued at USD 32,700 million in 2017 and…
7 Tips for Efficient Oncology Study Start-up
7 Tips for efficient study start-up: No.1) Involve Canadian oncologists early on and gather country-specific insight regarding possible enrollment…
Real World Evidence of a Successful Oncology Trial Rescue in Canada
Each clinical study presents unique challenges, and it’s not unusual despite every effort that a clinical trial does not proceed…
Canadian Know-How: Successfully Navigating a Centralized Framework for Oncology Clinical Trial Ethical Review
Now more than ever, time is of the essence when it comes to oncology clinical trial start-up and execution. The…
Canada: a Region of Choice for Your Study Expansion
Successfully designing and conducting oncology trials is not getting easier. Many of the challenges we are facing in oncology research…
Why Does Your CRO’s Assignment Practice for CRAs Matter?
Monitoring the progress of the research represents a fundamental aspect of successful outcomes by ensuring that constraints to success are…