The world's leading automated proofreading software

The 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?

Watch the webinar below, as we explore the why and how of a digital proofreading workflow.

Overview

Many organizations have made huge efforts to digitize several aspects of their business, but why not proofreading? The traditional proofreading process (manual proofreading) uses up a tremendous amount of precious human hours. If a mistake in regulated content is not identified, it can have a huge impact on patient safety and treatment efficiency.

Proofreading of regulated content in the pharma and medical devices industry is usually the responsibility of the person using the content to produce other materials. However, this long and error-prone task is only a small (but vital) part of the job, and not what many professionals have been trained for. Even the most highly trained and skilled professional proofreader reaches their limits during a working day, and this is when errors can go unnoticed.

Learning Objectives
  • Why proofreading is important to anyone working with Regulated Content
  • Why adopting a digital proofreading workflow is essential to remain competitive
  • How to guarantee data integrity with a digital proofreading workflow
  • Steps to implement a digital proofreading workflow
Who Should Watch
  • Regulatory Affairs
  • Regulatory Operations
  • Marketing/Ad/Promo
  • Quality Assurance
Presenters

Mike-Baird-Schlafender-Hase

Mike Baird
Director of Product Management

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.

Katarina Kresankova - web

Katarina Kresankova
Account Executive

Katarina is a sales professional with a Master of Arts focused in Translating and Interpreting. With a demonstrated history in business strategy and negotiation, she specializes in customer acquisition. She is also passionate about cooking, interior design and enjoys long runs.

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.

Past Webinars

January 17, 2024

Schlafender Hase Team

TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

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. 

August 23, 2023

Schlafender Hase Team

How to Build a Business Case for Document Comparison Software: A Step-by-Step Buyer’s Guide

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.

June 27, 2023

Schlafender Hase Team

Electronic Labeling is Here, How Are You Preparing?

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.