This one-day classroom course provides an interactive exploration of quality management systems and prepares you to build them in both site and sponsor settings to improve clinical trial operations efficiency and accuracy. ACRP’s on-demand eLearning Course, Building Quality Systems for Sites and Sponsors: Root Cause and CAPA, is included in your registration fee and is the pre-requisite, foundational learning for this classroom discussion of quality management systems from both site and sponsor perspectives.
This highly interactive one-day classroom course allows you to put risk assessment into practice through collaborative instructor-led group exercises such as scenarios and quizzes.
Expand your knowledge and skills in study protocol design and review. This e-Learning course covers the anatomy of a protocol, hypothesis development, study design, subject safety and data integrity risk considerations, protocol feasibility and protocol amendments.
Improve protocol interpretation and implementation by understanding trial scope, design, conduct, data analysis, and the evaluation and reporting of safety and tolerability data. This eLearning course explores the International Conference on Harmonization’s E9 guideline Statistical Principles for Clinical Trials.
Learn the key phases of the budget process and critical components required for consideration, including preparation and study protocol review, study start-up Costs and more. This eLearning course is ideal for both site and sponsor personnel who are tasked with building site budgets and reaching agreeable terms.