Thermo Fisher Scientific
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Join us virtually on October 15
LIVE WEBINAR: Transitioning Laboratory Equipment from Research and Development Work to GMP Compliance
Cell and gene therapy applications are projected to continue a global growth trajectory of more than 20% through 2024. Every year, more advances lead to new startup companies and partnerships. As you transition your discovery through research and development to commercial production in a GMP setting, your goal is to speed that process by minimizing variables. Laboratory equipment plays a key role in that process and should offer proven solutions.

This talk will:
  • Review the growth of regenerative medicine globally.
  • Provide an overview of GMP work and how it differs from basic research and development.
  • Explore the important ways that laboratory equipment can ease the transition including composition materials, factory acceptance testing, cleaning and maintenance, and factory trained support.

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Webinar details
LIVE WEBINAR: Transitioning Laboratory Equipment from Research and Development Work to GMP Compliance
Speaker: Mary Kay Bates, Senior Global Cell Culture Scientist
Date: October 15, 2020
Time: 10:00 a.m. SIN/HKG
Thermo Fisher Scientific