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From manuals to compliance: navigating regulations and documentation types in Life Sciences

  • Presentation
  • 12. March
  • 09:40 - 10:20 AM (CET)
  • Meeting Room 4+5
  • finished
  • Fosco Giordano

    Fosco Giordano

    • Cytiva

Contents

This session will provide an overview of key regulations and requirements in the Life Sciences industry, showcasing examples of content produced by Cytiva to meet customer demands.

Takeaways

Attendees will learn about major regulators and industry organizations in Life Sciences. The session will also cover the drug development process and highlight Cytiva's role in it. Additionally, it will address both direct and indirect customer requirements and explain how these translate into the documentation provided by Cytiva.

Speaker

Fosco Giordano

Fosco Giordano

  • Cytiva
Biography

I moved to Sweden in 2012 to start my PhD in Molecular Biology at Karolinska. During my thesis, I developed an interest in writing and illustration, which led me to a position as a technical writer at GE Healthcare (now Cytiva) in 2018. Since then, I have been working in technical communication. Recently, I transitioned to a support role, managing integration and exploring new tools in technical communication.

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