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From Concept to Cartridge: The Lifecycle of IVD Production

From concept to cartridge, in vitro diagnostic (IVD) production demands more than technical expertise – it requires precision, compliance and reliable scalability. Yet, developers often face obstacles like securing consistent, high-quality materials, navigating complex regulations and protecting against supply chain disruptions.

In this Teach Me in 10 episode, Dr. Lisa Fitzpatrick shares how Merck supports the entire IVD lifecycle – from R&D to commercial manufacturing – with production-grade components such as antibodies, enzymes, membranes and DNA-free reagents. She explains how Merck goes beyond supply, offering strategic partnerships, planning and scheduling support, custom manufacturing and the M-Clarity™ program for regulatory-ready documentation. 


Watch this episode to discover: 

  • The complete IVD lifecycle and critical material needs
  • How to overcome regulatory and supply chain challenges
  • Strategies to scale from R&D to market without compromising quality

Further resources:

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