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MilliporeSigma

A Molecule’s Journey

Break down roadblocks to clinical success and successfully build your own GMP biomanufacturing facility

Facility Engineering Services

Every biopharma executive must make important decisions early in clinical development that will impact their molecule’s journey – and ultimately the success of their commercial strategy. Our experts can help you navigate key considerations for designing, building, and operating an agile and flexible GMP biomanufacturing facility successfully, safely, and profitably.

Learn more with our guidebook, “Break Down Roadblocks to Clinical Success,” identifying how to overcome common roadblocks and navigate the complexities associated with:

  • Business planning
  • Technology
  • Regulatory and risk assessment
  • Facility engineering
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Your Trusted Partner

GMP biopharma manufacturing facility in Martillac, France

BioReliance® End-to-End Solutions facilitates success by providing our clients with flexible solutions and guidance based upon first-hand experience. Our in-house expertise building a fully single-use GMP biomanufacturing facility in Martillac, France, for example, can help you increase speed-to-market with a flexible, agile facility that features:

  • High-performance upstream and downstream systems
  • Industry-leading single-use technology
  • Rapid adaptation to changes in scope or strategy

Related Product Resources

Case Study: Building a Fully Single-use cGMP Biomanufacturing Facility in Martillac, France
Webinar: Key Considerations and Case Study for Building a cGMP Biomanufacturing Facility
Brochure: Optimizing and Executing Your Commercial Manufacturing Strategy

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