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TVT User Webinar: TVT Modules and TVT Connect

Published By:

Mike Baird

< 1 minute read

Covered in this webinar are best practices to:

Understand your needs: Select and use an automated proofreading software, designed for highly regulated industries
Improve your workflow: Optimize functionalities of TVT and the Spelling and Artwork modules in your workflow
Request TVT Connect: Automize error-prone, low-gain activities by connecting TVT to any of your information management systems

Who should watch this webinar?

TVT Users of all experience levels
Regulatory Affairs
Artwork Management
Packaging and Labelling Specialists
Quality Control Professionals

Presenter

Mike Baird

Mike is the Director of Product Management for Schlafender Hase. He is committed to continuously improving the existing software portfolio and at the same time also delivering new and innovative solutions to exceed customer needs. He has more than 25 years of experience working with global packaging, labelling, pre-media and artwork management leaders in the pharmaceutical and medical device sectors.

This webinar recording is available for TVT users in our TVT e-Learning portal.

After login, access your TVT X Essentials e-Learning course. The recording is under BONUS material.

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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Mike Baird

Director of Product Management, Schlafender Hase

Mike is the Director of Product Management for Schlafender Hase.

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Past Webinars

November 19, 2024

Schlafender Hase Team

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

< 1 minute read

The Game-Changing Features of TVT 12: A New Era in Compliance and Efficiency

TVT 12 is here! This annual update is packed exclusively with new features and improvements from customer requests that support key industry initiatives, boost efficiency, and add even more speed and detail to your document reviews.

October 30, 2024

Schlafender Hase Team

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

2 minutes read

How are increased compliance requirements impacting medical devices?

How are increased compliance requirements impacting medical devices? Discover the Future of Medical Device Regulation. We will dive into the rapid growth of the medical device sector, driven by cutting-edge technologies and rising regulatory requirements.

October 9, 2024

Schlafender Hase Team

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.

2 minutes read

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.