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Embracing e-Labeling in a global context

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Dr. Jutta Hohenhoerst
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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

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Learning the New Language of the EMA & The FDA: FHIR

Watch our interactive discussion session focusing on the evolution and outlook of Fast Healthcare Interoperability Resources (FHIR). FHIR represents a significant step in how we manage and exchange information and is rapidly gaining acceptance. In this session, industry experts will provide an introduction to the FHIR initiative, explore some current applications as well as the impacts, benefits and prospective timelines.