MAGI@home brings you and your team best-in-class, accredited training and education from the comfort of your home or office.
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For continuing education information click here.
sessions
CE credits
education
tracks
days
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: