Why Medical Device Manufacturers Must Look at the Bigger Picture When Implementing a GLS
Siemens and PRISYM ID discuss how standards-based interfaces in the global application landscape can make your labeling more efficient and agile
Global Labeling Systems (GLS) are becoming essential for many Medical Device Organizations. But thinking of a GLS as a standalone platform isn’t the answer. Without integrating labeling processes with Product Lifecycle Management (PLM) and Manufacturing Operations Management (MOM) platforms, management of your products’ data and label content will be far from seamless.
In roundtable session, experts from Siemens Digital Industries Software and life sciences label management specialists PRISYM ID explore how a fully integrated labeling solution can connect research and development (R&D) and manufacturing processes to ensure content is accurate and compliant at every stage in a product’s development.
Key Learning Objectives:
- Gain knowledge of best practice advice on integrated labeling system architecture and configuration.
- Understand why PLM, MOM, and GLS solutions are inherently linked and need to be closely aligned to ensure regulatory labeling compliance.
- Get insight into controlling process flows for synchronizing creation, approval and change of product and label data.
- Realize why integrating labeling as a core discipline is key to your manufacturing processes.
MEET THE PANEL
Jim Thompson, Ph.D.
Sr. Director, Industry Strategy, Medical Device & Pharmaceutical Industries, Siemens Digital Industries Software
Jim is the global industry leader for the Medical Device and Pharmaceutical industries at Siemens Digital Industries Software, helping Life Sciences customers get the most value from digitalization of their business processes using Siemens industry solutions, and guiding Siemens’ investments in Life Sciences industry-focused solutions.
Director of Medical Devices & Pharmaceutical Solutions, Siemens Digital Industry Software
Ryan Bauer is a product development strategist bringing medical device & pharmaceutical industry expertise to Siemens Digital Industries Software applications through tailored solutions in life sciences processes, practice, and regulatory compliance. After leading medical device R&D organizations for 13 years with additional experience in other regulated industries, Ryan knows where the pain points (and opportunities for improvement) exist to work smarter and transform industry practice.
Ryan has developed and launched a wide spectrum of medical devices including capital equipment, disposables (sterile & ready to use), re-usables, home use medical equipment, and smart devices for global markets. Additionally, he has helped lead ground-up rebuilds of medical device quality systems with successful global certifications and auditing.
Vice President of Strategic Accounts & Partner Ecosystem, PRISYM ID
Kevin Grygiel is Vice President of Strategic Accounts & Partner Ecosystem at PRISYM ID. He has over 15 years' experience in software development and implementation, helping to deliver complex and personalized business solutions to Life Sciences customers.
Kevin has a proven ability to focus, align and build effective teams with an uncompromising regard for customer impact. He also has the ability to conceptualize, develop and deliver innovative solutions and services that address and resolving enterprise-wide business needs resulting in a high degree of customer loyalty and retention.
VP Cloud Platform, PRISYM ID
Chris Lentz has been working at PRISYM ID for over 6 years, focusing on product management of PRISYM’s Cloud and Vision Inspection solutions.
With over 25 years’ experience in deploying and supporting enterprise software solutions across many sectors, Chris has spent the last several years bringing to market SaaS offerings that enable organizations to access high quality services based on leading software technologies.