The world's leading automated proofreading software

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

Published By:

Peter Muller
2 minutes read
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors

Table of Contents

Are you reviewing packaging materials, documents, submission documents, marketing materials etc. manually?

Have you already identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

As a buyer, identifying the initial support required in the proofreading process, through to making a final buying decision is a complex task. This is especially true when budgets are tight and every investment needs to be justified with a proven business case.

So how do you begin choosing the right content comparison software that will meet your existing and future needs?

Watch the webinar, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.  

Key Learning Objectives
  1. Understand how to align your team needs with the business needs
  2. How to define your proofreading challenges for your manager
  3. What are the best due diligence strategies to ensure you choose the ideal solution for your needs
  4. Learn to speak the language of your manager – Cost savings! 
Who should attend:
  • All stakeholders involved in researching, evaluating, proposing and selecting new technology tools
Presenters
Peter Muller, Schlafender Hase

Peter Muller
Sales Director North America

For over 25 years, Peter Muller has worked on software and process improvement projects relating to proofreading with Fortune 500 companies from various industries: Pharmaceutical, Medical Device & Consumer Goods. He has a wealth of experience working with international clients to define their organization’s goals and help them leverage new technologies to achieve productivity gains, process improvements and cost savings.

Dr. Jutta Hohenhoerst
Regional Sales Director, Schlafender Hase

Dr. Jutta Hohenhörst has more than 22 years experience in the pharmaceutical business. She has experience in different departments from Supply Chain Management to Strategic Marketing in F. Hoffmann-La Roche HQ, AstraZeneca and Fresenius HQ. While working for IQVIA during 2005 and 2012 she broadened her knowledge through strategic consulting projects in the pharma, medical device and hospital sector.

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.

Share this article

Peter Muller profile picture

Peter Muller

Director - Americas at Schlafender Hase

For over 25 years, Peter Muller has worked on software and process improvement projects relating to proofreading with Fortune 500 companies from various industries: Pharmaceutical, Medical Device & Consumer Goods.

Learn More

Subscribe to our blog

Are you reviewing packaging materials, documents, submission documents, marketing materials etc. manually?

Have you already identified the need for a solution to compare text and graphics in your organization, but need some help with the complete process of identifying, evaluating, and acquiring the right solution?

As a buyer, identifying the initial support required in the proofreading process, through to making a final buying decision is a complex task. This is especially true when budgets are tight and every investment needs to be justified with a proven business case.

So how do you begin choosing the right content comparison software that will meet your existing and future needs?

Watch the webinar, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.  

Key Learning Objectives
  1. Understand how to align your team needs with the business needs
  2. How to define your proofreading challenges for your manager
  3. What are the best due diligence strategies to ensure you choose the ideal solution for your needs
  4. Learn to speak the language of your manager – Cost savings! 
Who should attend:
  • All stakeholders involved in researching, evaluating, proposing and selecting new technology tools
Presenters
Peter Muller, Schlafender Hase

Peter Muller
Sales Director North America

For over 25 years, Peter Muller has worked on software and process improvement projects relating to proofreading with Fortune 500 companies from various industries: Pharmaceutical, Medical Device & Consumer Goods. He has a wealth of experience working with international clients to define their organization’s goals and help them leverage new technologies to achieve productivity gains, process improvements and cost savings.

Dr. Jutta Hohenhoerst
Regional Sales Director, Schlafender Hase

Dr. Jutta Hohenhörst has more than 22 years experience in the pharmaceutical business. She has experience in different departments from Supply Chain Management to Strategic Marketing in F. Hoffmann-La Roche HQ, AstraZeneca and Fresenius HQ. While working for IQVIA during 2005 and 2012 she broadened her knowledge through strategic consulting projects in the pharma, medical device and hospital sector.

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.

Subscribe to our blog

Past Webinars

E-labeling and what it means for regulatory teams

May 29, 2025

Schlafender Hase Team

RAPS Webinar: e-Labeling and what it means for Regulatory Teams

E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?

E-labeling and what it means for regulatory teams
2 minutes read

RAPS Webinar: e-Labeling and what it means for Regulatory Teams

E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?

TVT Integration Webinar

May 26, 2025

Schlafender Hase Team

TVT Integration: Connect, Automate, Accelerate

Learn how new custom integration capabilities make it easy to connect TVT with the systems you already use; enabling greater automation, reducing manual effort, and accelerating review processes, all while maintaining the precision and compliance standards you rely on.

TVT Integration Webinar
< 1 minute read

TVT Integration: Connect, Automate, Accelerate

Learn how new custom integration capabilities make it easy to connect TVT with the systems you already use; enabling greater automation, reducing manual effort, and accelerating review processes, all while maintaining the precision and compliance standards you rely on.

Esko Precision Talks Webinar

May 22, 2025

Schlafender Hase Team

Precision Talks: Optimizing Packaging Workflows with Compliance and Innovation

Join Chris Janczar from Esko and Marc Chaillou from Schlafender Hase for an exclusive discussion on how automation and digital maturity can transform your packaging workflows. This session is designed for professionals who are responsible for optimizing workflows, approving artworks, and reducing risk in their packaging process.

Esko Precision Talks Webinar
< 1 minute read

Precision Talks: Optimizing Packaging Workflows with Compliance and Innovation

Join Chris Janczar from Esko and Marc Chaillou from Schlafender Hase for an exclusive discussion on how automation and digital maturity can transform your packaging workflows. This session is designed for professionals who are responsible for optimizing workflows, approving artworks, and reducing risk in their packaging process.