Schlafender Hase Team
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.
Schlafender Hase Team
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
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.
Schlafender Hase Team
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.
Schlafender Hase Team
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
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
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
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
This webinar will help companies understand the nuances of global health authority drug product labeling requirements.
Schlafender Hase Team
This responsibility – to get everything right – often falls on Regulatory Affairs where the workload is high, and deadlines are short.
Schlafender Hase Team
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
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
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
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
After login, access your TVT X Essentials e-Learning course. The recording is under BONUS material.
Schlafender Hase Team
Eliminate your risk of misprints and perfect your pharma proofreading process by watching this webinar and using TVT.
Schlafender Hase Team
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
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.
