The Rythm of Research
Where Innovation, Collaboration, and Progress Unite
Join the clinical research community in New Orleans for MAGI 2027, where the rhythm of research comes to life. Inspired by the energy, creativity, and connection of the Crescent City, MAGI brings the industry together to share ideas, solve challenges, and keep progress moving. From emerging technologies and evolving regulations to operational excellence and collaboration, you’ll discover fresh perspectives, build meaningful connections, and stay in step with what’s next in clinical research.
Connections That Move Research Forward
In a city known for bringing people, ideas, and cultures together, MAGI creates its own unmistakable rhythm, setting the stage for sponsors, CROs, sites, technology providers, and industry experts to connect, exchange perspectives, and build meaningful relationships. Whether you're reconnecting with colleagues or meeting future collaborators, every conversation adds to the rhythm that keeps research moving forward.
Education That Delivers
Real-World Impact
Staying one beat ahead of evolving industry trends through expert-led sessions designed to provide practical insights you can apply immediately. MAGI's educational program features thought leaders from across the clinical research ecosystem and covers five education tracks: Budgets, Contracts, Billing Compliance, Clinical Operations, and Quality/Regulatory, with sessions focused on topics that matter most to today's professionals. Plus, attendees can earn up to X continuing education (CE) credits.
More Than a Conference Experience
Learning is important, but so is enjoying the journey. From puppy breaks and wellness activities to lively networking experiences and memorable moments, MAGI brings a little of the New Orleans spirit into every day. It’s a conference designed to engage, inspire, and leave you energized long after the final session.
A Track for Every Research Professional
Explore expert-led content across the subjects that matter most to your work and your organization.
Budgets
Learn the nuances of ensuring your site is optimized for conducting clinical trials by ensuring:
- Accuracy in budget forecasting.
- Effective negotiations.
- Timely payments.
- Efficient and effective resource management.
Contracts
Explore field-tested, easily implemented negotiation tools and techniques that can help you maintain control, improve turnaround times, and reduce last-minute scrambles including:
- Common pitfalls and how to avoid them.
- Key words that can significantly impact your contract.
- How to navigate a contract.
- Ensure data protection in your contracts.
Billing Compliance
Strengthen your research billing compliance development and program oversight by understanding:
- Advanced Coverage Analysis.
- Implications of anti-kickback, Stark, and false claims.
- How to operationalize your billing compliance process.
- Differences and similarities between medical device and drug development trials.
Quality/Regulatory
Understand and ensure adherence to the regulations on research participant protections, including:
- FDA and ICH regulations.
- Inspection readiness.
- Ethical review.
- Quality by design.
Clinical Operations
Master approaches to maintaining trial quality and effective tactics for protecting participant safety and data integrity, including:
- Engaging and optimizing hybrid trials.
- Diversity, equity, and inclusion.
- Maximizing operational efficiency.
- Optimizing protocol design and management.
