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.

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.

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term "Artificial Intelligence" will be discussed, and which might be desirable in a given context. 

Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

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.

Join Schlafender Hase as we discuss the challenges faced by life science companies when it comes to ensuring the accuracy of all digital and printed material and how technology can play an integral role in improving this process.

AI is already being used in many Life Science applications, meanwhile, Health Authorities are looking to regulate the use of AI. As a regulatory affairs professional, it is essential to have an understanding of this technology. In this general introduction to the field of AI, different uses of the term "Artificial Intelligence" will be discussed, and which might be desirable in a given context.

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.

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.

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. 

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.

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

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

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

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.

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.

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:

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

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

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

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.