Virtual | Sept. 23 -26, 2020

Featuring 100+ speakers presenting in 8 tracks with 26 different sessions/topics and also includes a robust exhibit and poster program.

This conference will assist clinical research professionals in improving their skills and understanding of the responsibilities of conducting clinical research in Canada.

This introductory course features two modules on clinical research regulatory and procedural practices and a medical/ scientific overview .

This one-day course will aid participants in preparing for the CCRP certification exam through review of FDA and ICH Good Clinical Practice (GCP) guidelines.

This conference will discuss current issues relating to compliance, development, and clinical investigation for Device Research. A Half-day optional Device Basics workshop precedes the main conference.

This two-day conference , jointly Sponsored with the FDA, will share information regarding clinical research regulations and GCP guidelines and discuss methods to aid the research professional in their practice.

This workshop, for site managers and research associates, will review billing, budgeting, profitability, and business best practices for clinical research programs.

This conference will aid the participant in understanding the legal, ethical and practical considerations related to human subjects research.

This course, for clinical investigators and key research staff, will review GCP, finance, budgeting and legal responsibilities of the clinical investigative site.

This interactive workshop, for site monitors, managers or auditors, will review GCP and clinical research monitoring best practices.

This two day program will cover the regulatory, financial, and ethical components of conducting clinical trials in the pediatric population.

This conference will review project management and risk management principles, budget development / financial management and global considerations for clinical research programs.

This workshop will discuss fundamental concepts and current issues in the development and implementation of an effective SOP program for clinical research and to decrease risk for clinical research sites, sponsors and Ethics Boards.

This workshop, for site coordinators, research associates, and study nurses with 0-5 years experience, will review the responsibilities at the clinical research site.