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Embracing e-Labeling in a global context

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Dr. Jutta Hohenhoerst
2 minutes read
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As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

Join experts Dr. Jutta M. Hohenhörst and Dean Halliday to unravel the impact of e-Labeling regulations. Explore the benefits for regulatory affairs professionals, understand the transition process, and learn tips for ensuring accurate content. Don’t miss this opportunity to stay ahead and drive positive change.

Key Learning Objectives
  •  The current status of e-labeling regulations
  • What are some of the top benefits of e-labeling
  • How e-labeling will impact the labeling & artwork process
  • Tips for ensuring accurate content and the importance of master source data
Presenters

Dean Halliday – Regional Sales Director, Schlafender Hase

Dean Halliday has been working with customers in highly regulated markets for over a decade and specialises in working with the Life Science Industry.

Ensuring that the related risks of manual proofreading and approval processes are identified and solved quickly and easily, allowing only approved content to be printed or published.

Dr. Jutta Hohenhoerst
Regional Sales Director, Schlafender Hase

Dr. Jutta Hohenhörst has more than 22 years experience in the pharmaceutical business. She has experience in different departments from Supply Chain Management to Strategic Marketing in F. Hoffmann-La Roche HQ, AstraZeneca and Fresenius HQ. While working for IQVIA during 2005 and 2012 she broadened her knowledge through strategic consulting projects in the pharma, medical device and hospital sector.

Do you want to find out more about how your proofreading life can be easier? Get in touch and we’ll tell you all about it.

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Dr. Jutta Hohenhoerst

Regional Sales Director, Schlafender Hase

Dr. Jutta Hohenhörst has more than 22 years experience in the pharmaceutical business.

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As the world shifts towards electronically delivered e-Labeling, it’s essential to stay ahead of the game. Regulatory Authorities are now permitting and encouraging online e-PIL content, with other regions follow suit.

Join experts Dr. Jutta M. Hohenhörst and Dean Halliday to unravel the impact of e-Labeling regulations. Explore the benefits for regulatory affairs professionals, understand the transition process, and learn tips for ensuring accurate content. Don’t miss this opportunity to stay ahead and drive positive change.

Key Learning Objectives
  •  The current status of e-labeling regulations
  • What are some of the top benefits of e-labeling
  • How e-labeling will impact the labeling & artwork process
  • Tips for ensuring accurate content and the importance of master source data
Presenters

Dean Halliday – Regional Sales Director, Schlafender Hase

Dean Halliday has been working with customers in highly regulated markets for over a decade and specialises in working with the Life Science Industry.

Ensuring that the related risks of manual proofreading and approval processes are identified and solved quickly and easily, allowing only approved content to be printed or published.

Dr. Jutta Hohenhoerst
Regional Sales Director, Schlafender Hase

Dr. Jutta Hohenhörst has more than 22 years experience in the pharmaceutical business. She has experience in different departments from Supply Chain Management to Strategic Marketing in F. Hoffmann-La Roche HQ, AstraZeneca and Fresenius HQ. While working for IQVIA during 2005 and 2012 she broadened her knowledge through strategic consulting projects in the pharma, medical device and hospital sector.

Do you want to find out more about how your proofreading life can be easier? Get in touch and we’ll tell you all about it.

Subscribe to our blog

Past Webinars

E-labeling and what it means for regulatory teams

May 29, 2025

Schlafender Hase Team

RAPS Webinar: e-Labeling and what it means for Regulatory Teams

E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?

E-labeling and what it means for regulatory teams
2 minutes read

RAPS Webinar: e-Labeling and what it means for Regulatory Teams

E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?

TVT Integration Webinar

May 26, 2025

Schlafender Hase Team

TVT Integration: Connect, Automate, Accelerate

Learn how new custom integration capabilities make it easy to connect TVT with the systems you already use; enabling greater automation, reducing manual effort, and accelerating review processes, all while maintaining the precision and compliance standards you rely on.

TVT Integration Webinar
< 1 minute read

TVT Integration: Connect, Automate, Accelerate

Learn how new custom integration capabilities make it easy to connect TVT with the systems you already use; enabling greater automation, reducing manual effort, and accelerating review processes, all while maintaining the precision and compliance standards you rely on.

Esko Precision Talks Webinar

May 22, 2025

Schlafender Hase Team

Precision Talks: Optimizing Packaging Workflows with Compliance and Innovation

Join Chris Janczar from Esko and Marc Chaillou from Schlafender Hase for an exclusive discussion on how automation and digital maturity can transform your packaging workflows. This session is designed for professionals who are responsible for optimizing workflows, approving artworks, and reducing risk in their packaging process.

Esko Precision Talks Webinar
< 1 minute read

Precision Talks: Optimizing Packaging Workflows with Compliance and Innovation

Join Chris Janczar from Esko and Marc Chaillou from Schlafender Hase for an exclusive discussion on how automation and digital maturity can transform your packaging workflows. This session is designed for professionals who are responsible for optimizing workflows, approving artworks, and reducing risk in their packaging process.