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API Regulatory Roadmap


Navigating the Complicated World of Global Approvals

Navigating the complicated world of global approvalsBringing a new drug to market – and keeping it there – can be a long and complicated journey.  The path in which companies navigate regulatory challenges can mean the difference between first-to-market success and cost overruns. At Merck, we have been setting standards in regulatory services for many years and understand the responsibilities you face.

Our regulatory competencies enable you to:

  • Speed approval preparation and extend compliance
  • Simplify your qualification processes and reduce stress
  • Increase supply chain transparency and reliability
With our extensive regulatory know-how coupled with chemical and pharmaceutical expertise, we offer a comprehensive range of APIs, excipients, and services that help you get your product to market more quickly. Our worldwide presence and dedicated teams keep us –and you - one step ahead because we constantly review regulatory developments in all relevant markets.

For more information, please click here to read our brochure.

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Webinar: Formalized Risk Assessment: Challenges and Best Practices - Watch Now

Webinar:
Formalized Risk Assessment: Challenges and Best Practices

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Your fast track through regulatory challenges. The new Emprove® program. Learn More

Your Fast Track Through Regulatory Challenges.
The new Emprove® program.

Learn More