Lean Authoring Checklist

Lean Authoring Checklist

Lean Authoring: Eliminating Redundancies And Complexities For The Pharmaceutical Industry And Health Authorities

DOWNLOAD the Lean Authoring Checklist

Thinking there must be a better way forward on regulatory submissions to reduce repetition, save time and streamline the process?

It’s no wonder there is frustration given critical information locked into PDFs, repetitive files being sent, and lack of standardization on content. This outdated approach places an unnecessary burden on both the pharmaceutical companies and the Health Authorities.

It’s time to optimize the outcomes through Lean Authoring – a more effective way to standardize and accelerate the overall submission process in the pharmaceutical industry.

Content Has Evolved

Learn best practices to lean authoring to unlock your data and streamline regulatory processes to Health Authorities.

Lean-Authoring

Discover how Lean Authoring helps:

  • Standardize submissions to separate out tables from text and reduce the amount of text
  • Reduce turnaround time with optimized workflows and streamlined information that can be reused multiple places
  • Achieve cost savings by eliminating redundant information and documents
  • Increase efficiency and give your team back time for more strategic work such as new product development

In this checklist, you’ll have a practical guide on how to reframe content to provide the right context. We provide you with actionable steps including:

  • 1
    How to structure the data
  • 2
    Specific examples comparing long prose to tabular formats
  • 3
    Detailed checklist on what to include in your content
  • 4
    Mindset change and approach, align throughout the company

Download now to unlock your access to the Lean Authoring Checklist and discover actionable steps to streamline your regulatory submissions.

"*" indicates required fields

Name*
Hidden
Hidden
Service
Hidden
Website Lead Gen
This field is for validation purposes and should be left unchanged.