MAGI@home 2026 brings you and your colleagues the most value to overcome challenges during disruptive times.
This year's virtual conference delivers best-in-class, accredited training and networking opportunities to propel your research goals despite current constraints and challenges. Gain insights and new ideas as we come together and navigate success.
All sessions have been recorded recorded and available on-demand until October 2027. You can listen at your own pace and still get the CEUs you need!
sessions
CE credits
education
tracks
days
per person
sessions
days
CE credits
educational
tracks
per person
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:
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: