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Find out why we are the proven leader in Risk Evaluation and Mitigation Strategies (REMS)

No matter the complexity of your REMS requirements, balancing the demands of the FDA with the need for timely and appropriate access to your brand is key to your success. McKesson Specialty Health does it every day.

McKesson Specialty Health is setting the industry standard for how REMS are designed and managed. We have the expertise and tools to develop REMS programs that deliver on the commitment made to the FDA, while integrated into the existing workflow of stakeholders. Our technology and reach are unmatched, thus allowing us to build FDA-approved solutions that ensure safe access to REMS medications.

Our team of experts works with companies like yours to secure FDA approval for new products coming to market as well as modifying and improving existing risk management programs.

Why put your product at risk? Choose the market leader who is setting the standard on all fronts; from REMS consulting and submission, to execution, inspection readiness and client relationships. We'll be with you every step of the way to provide the comprehensive services you need to ensure your success. Find out what our many customers already know.

To learn more about our offerings, CONTACT US for more information.

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