MAGI 2025

Registration is now open!

Whether you are a clinical research novice or veteran, work with a study sponsor, research site, or CRO, MAGI 2025 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 2025 in Boston are:

Earning up to 19 continuing education hours in person and up to 68.5 more if you listen to all the recorded sessions.
Participating and engaging with CRA’s, CRCs, folks from clinical operations, contracting, finance, and clinical affairs.
Exploring our exhibit floor with great solutions to many of your problems.
Being part of the voting in our annual Innovation Challenge or better still, submit an idea to the challenge and potentially present it live!
Getting in-depth training with our Sunday workshops and potentially earning a GCP Training certificate accepted by the TransCelerate Mutual Recognition (MR) Program.
Increasing your personal development with our Wednesday morning programming.
Experiencing fewer distractions so you can focus on the content and the networking.
Relaxing with our early morning yoga sessions.
And, of course, did we mention the puppies?

MAGI 2025 education tracks:

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.

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.

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.

The WCG Innovation Challenge is returning to Boston! Don’t miss the opportunity to participate in this fun — and valuable — challenge. Listen to research professionals present the inventive ideas they’ve come up with related to clinical trial site efficiency, increased performance or quality improvement.

Register now and join us in Boston.

Registration Fee Schedule