Webinar Objectives:
Practical Considerations for Conducting Clinical Trials in Canada
Gain a clear understanding of the essential steps and strategies to navigate the Canadian clinical trial environment successfully, including regulatory requirements.How to Plan and Budget for a Clinical Trial
Learn effective techniques for creating comprehensive trial plans and budgets, while accounting for key factors.Support Services and Resources Available
Discover the array of support networks and resources in Canada designed to streamline the trial process and foster collaboration.
Meet the Speakers!
Breanne Stewart (BSc, BScN, RN) serves as the Network Director for RareKids-CAN: Pediatric Rare Disease Clinical Trials and Treatment Network- she provides strategic leadership, oversees operations, and drives collaboration within the network. With a focus on shaping RareKids-CAN's direction, Breanne is dedicated to fostering partnerships and ensuring the delivery of high-quality clinical trials and innovative research initiatives for individuals affected by rare diseases. Having joined MICYRN in 2018 as the inaugural Associate Director of Clinical Trials, Breanne is deeply passionate about optimizing research processes in Canada to ensure timely and efficient treatment and access to therapies for patients and their families.
Lori Anderson has spent the past 20+ years acting as a Health Canada Regulatory specialist working with academic institutions, researchers, and third-party groups to facilitate the submission of high quality applications to TPD, BRDD, NNHPD and the Medical Devices Directorate. She has also collaborated on submissions with national research networks and industry partners. In addition, Lori has 10 years of experience as a clinical research associate in the field of Cardiology, which has contributed greatly to her knowledge, passion, and expertise in clinical trial design, regulations, and conduct.