Moving From Documents to Data: Improving Management and Traceability of Critical Data in Medical Device Manufacturing

Medical Device, Medical Device Safety and Regulation, Medical Device Manufacturing & Supply Chain,
  • Wednesday, January 29, 2020

Medical device companies are subject to regulatory and compliance demands related to their products and development process. Often, that leads to a huge amount of data being produced in the form of documents and other data types.

Managing this data is not easy, because the location, as well as the context of the documents and related data, need to be managed. This is often where the problem occurs. And it gets even worse when you need to share your data or submit packages externally.

Many medical device manufacturers are looking for better ways to structure and manage their documents so they can meet regulatory or compliance requirements.

Minerva has worked in regulatory and compliance heavy industries for decades, and in this webinar, the featured speakers will share their experiences and ways to address the challenges device manufacturers face by utilizing digital data to drive business process transformation.


Jennifer Moore, Minerva Group

Jennifer Moore, Business Development Director, Minerva Group

Jennifer Moore is an entrepreneurial thinker with extensive experience in developing and deploying large, multi-faceted enterprise software projects, leading cross-functional teams, navigating sophisticated environments and driving revenue as well as market adoption. She has more than 15 years of experience in business transformation across various industries including medical device.

Message Presenter
Oliver Dick, Customer Relationship Manager

Oliver Dick, Customer Relationship Manager

Oliver Dick combines several years of experience in the field of product lifecycle management (PLM) software in a regulated environment with a deep knowledge of the global medical device industry. He is an engineer by training and has engineer working experience from medical device companies such as Dräger, Pulsion and Olympus Surgical Technologies. His specialties include best practices on verification engineering and regulatory compliance.

Message Presenter
Thomas Skogen, Minerva Group

Thomas Skogen, Product Director, Minerva Group

Thomas Skogen brings experience from his background in supply chain and manufacturing optimization, where he has helped several global companies optimize their internal and external business processes. Thomas’ experience originates mainly from the electronics & high-tech and medical device industries. This combined with his experience within all levels of PLM implementations provides a solid foundation for his current role of managing customer engagement and development of Minerva’s product range targeted towards electronics & high-tech and medical device industries. Thomas comes with a background as an electronics engineer, complemented with a Master’s in Technology Management. Thomas has held positions in multinational corporations such as Nilfisk, heading the internal optimization programs as well as the supply chain organization.

Message Presenter
Christoph Golinski Senior PLM consultant

Christoph Golinski, Senior PLM consultant

Christoph Golinski has more than 15 years of experience in consulting for PLM solutions in the medical device, aerospace, electronics, high-tech and renewable energy industries. His knowledge spans the disciplines of configuration management, requirements engineering and PLM data quality management. His fascination of PLM software is visible, and he could talk about it for hours. The range of requirements and the tools used in a manufacturing company is wide and almost everything is included in a PLM software system, from complete in-house developments to open source. The character of the product data and the business processes vary from heavily regulated industries to less regulated industries, but both will benefit from being managed in a PLM system. In short, PLM is and remains the backbone of every industrial company.

Message Presenter

Who Should Attend?

This webinar is targeted at directors and upwards in the following business areas:

  • Engineering
  • Quality
  • Design
  • Regulatory
  • Development

What You Will Learn

Participants will learn:

  • How to improve efficiency in controlling and managing complex data structures
  • How to secure and improve traceability
  • How to improve visibility and processes
  • How to secure a complete audit trail in one system

Xtalks Partner

Minerva Group

Minerva Group is one of the most established vendors of Product Lifecycle Management software solutions for the medical device industry. Our industrial solutions and add-ons for the Aras Innovator software platform help our clients to speed up the implementation process. With Medical Device PLM, we support medical device manufacturers to optimize their processes, projects and information management by handling everything concerning the product, from cradle to the grave. Read more at or

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