Whitepapers & Webinars

Seabrook’s highly-requested webinar series and professional whitepapers are now available, on-demand, straight to your inbox. 
To access these resources, visit the links below and complete the appropriate request. 

Please allow 24 hrs. for your request to be processed.  

Whitepapers & Webinars

by | Jan 9, 2020

Upcoming Live Events: Hosted by Seabrook

Professional Whitepapers: Delivered To Your Inbox

WHITEPAPER 1:
What Digital Transformation Means for Medical Device Manufacturers

This white paper outlines the need for medical device manufacturers to evolve their business practices by transitioning from paper-based processes to digital in three main areas: business, technology and regulatory. To achieve success in today’s environment, organizations must commit to adopting innovative approaches to facilitate the development of next-generation medical technology (med-tech) manufacturing.  Presented by Siemens. 

Request this whitepaper.

WHITEPAPER 2:
Enabling Closed-Loop Manufacturing in the Medical Device Industry

Siemens presents a whitepaper on the benefits of implementing closed loop manufacturing into the Medical Device and Diagnostic Industry.  As a Siemens technology sales partner, Seabrook Technology Group improves customer business processes and manufacturing efficiency by sharing knowledge and supporting operational excellence. Our focus is on the use of modern technology and software for business optimization. This whitepaper is of relevance to those in medical device manufacturing. 

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WHITEPAPER 3:
Paperless Manufacturing Required to Achieve Operational Excellence Through a Smart Factory

Standards, regulation and greater levels of competitiveness are changing the medical device manufacturing industry.  Further industry drivers include demand for electronic medical records for collaboration and improved patient care. Increasingly stringent standards place a requirement on medical device manufacturers to produce more detailed labeling, dating, use-by dates, sourcing, detailed manufacturing records and accountability – yet, many medical device manufacturer floors are paper-driven. This operation simply cannot compete efficiently and effectively while in compliance with new regulation. This whitepaper will explore how paperless manufacturing can lead to operation excellence through the implementation and investment in a factory of the future. 

Request this whitepaper.

Receive Access to On-Demand Webinars

NEW! WEBINAR 1:
Paperless Manufacturing: Process Changes and Quality Control for Medical Device Manufacturers

Webinar series one highlights the journey of implementing Paperless Manufacturing. In it, we discuss the benefits that implementing Paperless Manufacturing can bring, including the elimination of DHR errors and the simplification of FDA audits. Hosted by Seabrook’s resident MES experts.

WEBINAR 2:
Paperless Manufacturing: Building a Case for Paperless Manufacturing

Seabrook’s second webinar series helps organisations to understand how to enable operational excellence utilizing a Manufacturing Execution System. Covering topics such as paperless manufacturing, improving manufacturing performance, and creating a road map for implementation, this webinar is hosted by Seabrook Technology Group experts.

WEBINAR 3:
Keeping Pace with Change in MedTech: Challenges and Solutions

Presented by the manufacturing technology experts at Siemens.   Discover MD&D industry challenges identified by Axendia and the benefits and solutions provided by Siemens Opcenter Execution for Medical Device manufacturers.

WEBINAR 4:
Scale Up Manufacturing & Enforce Compliance (and Quality) with MES Implementation and Rapid Implementation Methodology

This webinar is specifically designed for medical device manufacturers looking to rapidly increase production.  This brief presentation discusses the advantages of MES implementation, the FDA’s “Case for Quality,” and the utilization of Rapid Implementation Methodology to scale-up production quickly.

WEBINAR 5: 
FDA and Edwards Lifesciences Collaboration for Quality Excellence

Discover the role of FDA initiatives around product quality excellence and learn how MedTech manufacturers are adopting them.  Medical device manufacturers should focus on innovating, producing and delivering high-quality devices proactively with regulatory compliance being a baseline.  Edwards Lifesciences has joined the FDA in its strategy and adopted a proactive approach to product quality excellence.  Presented by Siemens Manufacturing Technology experts.

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With a reputation built on thirty years of succeeding together with our partners, we are a team of manufacturing technology experts and industry thought leaders bringing end-to-end manufacturing solutions (people, processes, and technology) together to enable operational excellence for medical device and biotech manufacturers.

North American Contact:

Seabrook Technology Group
600 Corporation drive, Suite 108
Pendleton, IN 46064
+1 317-426-0699

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Seabrook Technology Group
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+353 21-4800-840