Prepare for an ACRP Certification with this comprehensive guide. This eLearning course will help you become familiar with the exam format, tackle example questions, and conduct a personal gap analysis to ensure you are fully primed to earn your ACRP Certification.
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.
As an investigator, do you know what risk-based monitoring (RBM) means to you and your trial staff? This interactive eLearning course answers the fundamental questions: What is RBM and how is it different from the standard monitoring approach? It also examines the impact on investigators specifically, including new approaches to data management, study budget and contract considerations.
Become an expert on quality and risk-management strategies and procedures. This eLearning course answers the fundamental questions: What is risk-based monitoring (RBM) and how is it different from the standard monitoring approach? It then examines the impact on CRCs specifically, including new approaches to data management, study budget and contract considerations.