Webinars | Schlafender Hase

Schlafender Hase Team

Digitizing the Proofreading Workflow: A Game Changer for Professionals in Life Sciences

Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.

Schlafender Hase Team

Level Up with TVT 11

Just when you thought TVT couldn’t get any better, TVT 11, the most powerful version ever is set to be released on November 8th 2022.

Schlafender Hase Team

E-PIL Legislation: The Impact on Patient Safety, Accessibility and Environmental Sustainability

Providing patients and Health Care Practitioners with electronically delivered e-Labelling is becoming increasingly important. Several Regulatory Authorities now permit and encourage online e-PIL content, with other regions following suit.

Schlafender Hase Team

Webcast: e-PIL legislation will have a positive impact on patient safety and sustainability

Ensuring content is delivered accurately in print and online formats, will be vital to ensuring patient safety, especially during the complex transition phase from printed-paper to electronic patient information.

Schlafender Hase Team

Innovator Rx Drug Product Labeling 101: From Creation to Change Management

This webinar will help companies understand the nuances of global health authority drug product labeling requirements.

Schlafender Hase Team

Labelling Issues & Opportunities for UK Operators

This responsibility – to get everything right – often falls on Regulatory Affairs where the workload is high, and deadlines are short.

Schlafender Hase Team

Effective Labeling Management Requires a New Mindset

Watch our sponsored webcast with RAPS, led by Cham Williams: Effective Labeling Management Requires a New Mindset: A Strategic Guide to Labeling Process Optimization.

Schlafender Hase Team

Future Proof Your Regulatory Submissions for Global Compliance

Data Management is an integral part of regulatory compliance across the globe. There are many nuances to consider including information storage, change management, and measurable evolution of harmonious systems.

Schlafender Hase Team

Webinar: Make Sure Your Barcode Makes the Grade

In this webinar you will learn how TVT Barcode identifies barcode errors before they are printed and automatically detects, decodes, compares and grades barcodes used by highly regulated industries like Life Science.

Schlafender Hase Team

Vaccinate Your Workflow to Eliminate Labelling Errors

Listen to the 30 minute webinar to find out all the best practices to prevent errors and what to do if you suspect artworks may be infected with errors:

Schlafender Hase Team

TVT User Webinar: TVT Modules and TVT Connect

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

Schlafender Hase Team

Proofreading in the European Pharma Industry: Challenges and Misconceptions

Eliminate your risk of misprints and perfect your pharma proofreading process by watching this webinar and using TVT.

Schlafender Hase Team

What You Need to Know About the EU MDR. Are You Ready?

Watch this webinar to learn how the EU MDR will impact the medical device labeling process and how you can best prepare.

Schlafender Hase Team

Hidden Risks in Your Packaging & Labeling Artwork

There are many potential issues with labeling artwork design proofs. Most of these issues are visible to the human eye when reading through the document, but a few of them are invisible and require special techniques to find. In this webinar we uncover hidden problems that can lead to additional correction cycles or even misprints.