
Whether you are a clinical research novice or veteran, work with a study sponsor, research site, or CRO, MAGI 2026 will offer best-in-class educational opportunities for all career levels to support your continuing education and your professional growth and success.
The benefits of attending MAGI 2026 in Chicago are:

Strengthen your research billing compliance development and program oversight by understanding:

Learn the nuances of ensuring your site is optimized for conducting clinical trials by ensuring:

Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, including:

Explore field-tested, easily implemented negotiation tools and techniques that can help you maintain control, improve turnaround times, and reduce last-minute scrambles including:

Understand and ensure adherence to the regulations on research participant protections, including:

Learn the nuances of ensuring your site is optimized for conducting clinical trials by ensuring:

Explore field-tested, easily implemented negotiation tools and techniques that can help you maintain control, improve turnaround times, and reduce last-minute scrambles including:

Strengthen your research billing compliance development and program oversight by understanding:

Understand and ensure adherence to the regulations on research participant protections, including:

Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, including:

Learn the nuances of ensuring your site is optimized for conducting clinical trials by ensuring:

Explore field-tested, easily implemented negotiation tools and techniques that can help you maintain control, improve turnaround times, and reduce last-minute scrambles including:

Strengthen your research billing compliance development and program oversight by understanding:

Understand and ensure adherence to the regulations on research participant protections, including:

Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, including: