DIA Canadian Annual Meeting
Highlights & Features
What is happening at DIA Canadian Annual Meeting
As a new edition to our programming this year, our pharmacovigilance track will provide a comprehensive overview of Canada’s regulatory environment in the field of clinical safety and pharmacovigilance for biopharmaceutical products and medical devices. Our pharmacovigilance track will kick off with an overview from representatives of various regulatory agencies, where they’ll share lessons learned from COVID-19 and their thoughts on the future challenge of risk-management planning in a post-pandemic world. Subsequent sessions will cover topics such as good pharmacovigilance practices (GVP) inspections, post-market surveillance, the use of artificial intelligence in pharmacovigilance, and general data protection regulation (GDPR) and its implications.
Gain a clearer understanding of Canada’s regulatory landscape through our regulatory track. You’ll hear about Health Canada’s modernization initiatives with complementary perspectives from industry on advanced therapeutic products (ATPs), medical devices, good manufacturing practices (GMP) virtual inspections, pediatric medicines, and international collaborations.
Today, modern biopharmaceutical and device products are advancing at an unprecedented speed. Sessions in this track will focus on clinical research development and operations for industry. Those interested in this track will gain an understanding of Health Canada’s approach to the modernization of clinical trial regulations, including case studies of how patients have contributed to resource development and how decentralized trials have the potential to transform the way we conduct clinical research. Take your level of understanding a step further and explore our other sessions including an industry perspective on good clinical practices (GCP) in relation to clinical trial site GCP audits and clinical trial compliance (CTC) inspections. Our attendees in this track will be able to gain real-world insights into the benefits and challenges of incorporating real-world data and real-world evidence into a whole range of decisions about clinical trials.
Preconference Short Course
- Short Course 1: Introduction and Update on Eurasian Economic Union Regulatory Environment and Electronic Drug Registration Format October 18 | 9:30AM-12:20PM
Upon completion of registration, participants will gain access to the following:
- Live Event Access
- Presentation Slides
- Access to recorded sessions, on demand for 4 months post event
As global events continue to accelerate the shift to digital meeting formats, the ways in which we collaborate have also evolved. Here are three key reasons to consider attending a virtual DIA Specialty Event!