MAGI@home (October 16-20, 2023) brought you best-in-class, accredited training and education from the comfort of your home or office.
Thank you to all of you for attending the event and a big thank you to our great faculty of speakers. All 46 accredited sessions are available for you to view in the On-Demand section of the site.
For continuing education information click here.
If you want to use the questions from our daily quiz, you can download those here.
We're back in person in the spring. We will be visiting the great city of New Orleans, April 14-17, 2024. More information will be posted here in the coming days.
sessions
CE credits
education
tracks
per person
days
hours
per day
CE credits
education
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:
Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, 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:
Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, including:
Understand and ensure adherence to the regulations on research participant protections, including: