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Catalent Acquires Premier European Product

Launch Site from Bristol-Myers Squibb

Catalent recently announced the completion of the acquisition of the Bristol-Myers Squibb’s biologics, sterile, and oral solid dose product manufacturing and packaging facility in Anagni, Italy .

 

The state-of-the-art facility designed for late-phase tech transfers and commercial product launches has a track record of launching hundreds of new products across many therapies including cardiovascular, cancer, and hepatitis treatments.  This facility will provide Catalent customers access to:

  • Comprehensive commercial packaging solutions with blister and bottling capabilities
  • Serialization solutions to ensure product traceability throughout the global supply chain
  • Integrated digital printing and RFID tracking, enabling 48-hour turnaround to market
  • Highly automated warehousing


The Anagni facility complements Catalent’s existing European oral solid dose development and manufacturing network in:

 

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Article: Planning Successful Product Launches

Developing and bringing a new drug to market is a long, expensive and uncertain process. Read this article published by Pharmaceutical technology to learn about proven strategies for a successful product launch, including cross-functional team collaboration, risk management and using the right project management tools.


Webinar: Flexible Manufacturing Strategies:

What’s Best for Your Product?

Pharmaceutical and biotechnology companies approach external development and manufacturing partners for solutions for their product’s specific needs.  New products are increasingly complex and must be developed in shorter timelines to meet patient needs.  With the rise in accelerated designations (i.e., orphan drugs, fast track, etc.), advanced manufacturing technologies and smaller batch sizes are becoming the trend. 


Brochure: Customized Manufacturing Solutions

Manufacturing pharmaceutical, biologic and consumer health products is becoming ever more challenging. With more complex molecules, accelerated timelines, global requirements and regulatory complexities, planning for a scalable clinical solution, a successful launch and reliable commercial supply is a critical and complicated task. Learn how Catalent has the scale, the experience and the capacity across multiple dose form delivery technologies and global regions to meet your complex manufacturing needs and supply better treatments for your patients and consumers.


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