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 This outdated approach places an unnecessary burden on both the pharmaceutical companies and the Health Authorities.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.
Download now to unlock your access to the Lean Authoring Checklist and discover actionable steps to streamline your regulatory submissions.
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
How to structure the data
Specific examples comparing long prose to tabular formats
Detailed checklist on what to include in your content
Mindset change and approach, align throughout the company
For further regulatory assistance or queries on how Celegence can support your organization, reach out to info@celegence.com today.
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