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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 Millipore, 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