The Role of Ethics from a Clinical Research Associate’s Perspective: Patient-Centered Research
A contract research organization (CRO) functions as the intermediary between a biopharma company sponsoring clinical trials and the research sites…
Hassle-Free Site Selection and Study Start-up for Clinical Trials in Canada
It is no secret that Canada’s presence as a key player in the field of pharmaceutical drug development is rapidly…
Do You Believe the Myths About Conducting Clinical Trials in Canada?
Myths exist to explain things we don’t understand, as well as to continue traditions and keep relationships and societies ‘safe’.…
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…
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…
How Does Your CRO’s Feasibility Process Contribute to Your Clinical Trial Success?
In clinical research, the process of finding and selecting sites is essential to the success of a study, as it…
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…