In this workshop, you'll gain a solid understanding of the fundamental considerations for DCTs and learn practical approaches to designing, administration, and implementation.

Aids participants in preparing for the CCRP certification exam through review of FDA and ICH Good Clinical Practice (GCP) guidelines.

Presents project management and risk management principles, budget development / financial management and global considerations for clinical research programs.

This workshop, for site coordinators, research associates, and study nurses, will review the responsibilities at the clinical research site.

 This conference provides attendees with new information, tools, and real life examples to help participants navigate the components of quality management in clinical research - quality planning, quality control, quality assurance, and quality improvement.

Shares information regarding clinical research regulations and GCP guidelines and discusses methods to aid the research professional in their practice.

Covers the regulatory, financial, and ethical components of conducting clinical trials in the pediatric population.

Discusses current issues relating to compliance, development, and clinical investigation for Device Research.

Assists Research Professionals in improving their skills and their understanding of the responsibilities of conducting oncology clinical research.

Assist in improving skills and understanding of the practical financial and business tasks related to clinical research.

Reviews GCP and clinical research monitoring best practices for site monitors, managers or auditors, in an interactive format. 

Presents the essential functions of the clinical research nurse with consideration of the recently released ANA Scope and Standards of practice for Clinical Research Nursing.

Assists Research Professionals in improving their skills and their understanding of the responsibilities of conducting clinical research in the emergency setting.