How to survive Medtech’s exponential growth in content

16 March 2021 | 4:00 PM EST | Online

Catch the latest updates on how and why you should adopt a centralized content managed methodology to efficiently organize high volumes of data.

Medical device makers are in charge of producing extensive levels of documentations to meet regulatory requirements and to get products on the market in a timely fashion.

In order to meet the demanding expectations of MDR and other new regulations, your organization necessitates an efficient strategy and system to work through.

Many medical device companies still used decentralized approaches that lack strategy, automated workflows and changed managed which is required for a high performing and streamlined product development life cycle.

Join us on March 16 for real-world examples of success when adopting a Content Management methodology that addresses these needs by utilizing an efficient and streamlined solution that significantly reduces time to market.

Why attend?

In this webinar, you’ll learn about:

  • Why medical device makers need an air-tight strategy
  • Which content challenges are unique to Medtech
  • What an integrated content management solution means


Devicetalk webinar

16 March | 4 pm EST

Meet the Speakers

Gilles Beaugeais

 Structured Content Business Consultant, Amplexor  

Gilles Beaugeais began his career at Syselog working as a developer and throughout the years, he was able to build a foundation that led to solid expertise on XML-related standards, technologies and softwares. Having worked for many aeronautic companies, he’s been able to provide expertise on ATA and S1000D standards, as well as on interactive publication strategies, systems rationalization (via audit) and best approaches for CMS integration. Gilles’s most recent challenge has been in the medical sector for a leading medical device company, consisting of defining and validating scenarios to replace manual processes that would allow the publishing of multilingual documents using InDesign by automated processes using XML and the DITA standard. He now works at Amplexor as a Structure Content Business Consultant. 

Dan Schneider

Business Development Director, Amplexor

An entrepreneur and business problem-solver at heart, Dan Schneider is Sr. Business Development Director at Amplexor Life Sciences, where he helps N. American and global medical device and pharmaceutical companies adopt innovative solutions to reduce the time and cost to develop and release multilingual IFUs and other product documentation. As the founder of two successful companies, one in Japan and one in California, Dan understands the importance of streamlining processes to gain operational efficiencies and reduce time to market. He’s passionate about his work and Dan thrives on working closely with his clients to help them improve their business performance. Dan is the proud father of three daughters, and he and his wife Jackie enjoy the outdoors and travelling.