Upcoming Webinars and Events.
DIA RSIDM 2025
DIA’s annual regulatory submissions, information, and document management forum
3 click document compliance
All that valuable time you spend on ensuring submission-readiness for documents (bookmarks, hyperlinks, table of contents, fonts, PDF properties, etc.) and then validating the output, can be much, much faster.
Going from hours to a matter of minutes. Here’s how it would look like:
1️⃣ Select Word or PDF documents you want to include in a US FDA submission
2️⃣ Drop these documents in a web browser
3️⃣ Get FDA compliant output in a matter of seconds.
Did you miss a webinar?
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How to save time in document prep.: Replacing desktop PDF tools with automation
Thursday, Dec 5, 2024
6:00 PM GMT+1
Best Practices in PDF preparation automation
Manual PDF prep challenges?
What can be automated?
What are the benefits for you?
Wednesday, 27 March, 2024
11:00 AM CET
How to create compliant PDFs & reports from a browser in 3 clicks with DocShifter
With a 15-minute practical demo.
Wednesday, 27 March, 2024
11:00 AM CET
3-click document compliance for CRO & Regulatory Service Providers
Including a practical demo.
Wednesday, 27 March, 2024
11:00 AM CET
How to automate PDF rendering for global submissions with DocShifter
Including a practical demo.
Thursday, 8 June, 2024
6:00 PM CET
How to render Veeva binders with DocShifter into submission-ready PDFs
And other content automation.
Wednesday, 27 March, 2024
11:00 AM CET
How to automate document preparation & report generation in Veeva with DocShifter
Thursday, 27 April, 2024
11:30 AM CET
How to simultaneously render compliant PDFs for your global submissions
Including a 15 minute practical demo.
Friday, 13 January, 2023
11:30 AM CET
How to accelerate content preparation for regulatory submissions: A case study by Pharmalex
How can you automate many of your manual steps in submission content preparation, and how did Pharmalex do it?
Thursday, 21 April, 2022
5:00 PM CET
Lessons Learned on Document Preparation in Life Sciences
Abstract from the DIA Regulatory Submissions, Information and Document Management Forum 2022.
Friday, 26 August, 2022
11:30 AM CET
How to auto check and fix Word and PDF documents for compliance
Thursday, Sep 26, 2024
6:00 PM GMT+2
How to accelerate content preparation for regulatory submissions: A case study by Pharmalex
How can you automate many of your manual steps in submission content preparation, and how did Pharmalex do it?
Thursday, 21 April, 2022
5:00 PM CET
How to create compliant PDFs & reports from a browser in 3 clicks with DocShifter
With a 15-minute practical demo.
Wednesday, 27 March, 2024
11:00 AM CET
3-click document compliance for CRO & Regulatory Service Providers
Including a practical demo.
Wednesday, 27 March, 2024
11:00 AM CET
How to automate document preparation & report generation in Veeva with DocShifter
Thursday, 27 April, 2024
11:30 AM CET
How to save time & reduce risks by fully automating the creation of your reports
IMPD, CSR, SOP, annual reports, 510k & PMA submissions and many more.
Friday, 4 November, 2022
11:30 AM CET
How to render Veeva binders with DocShifter into submission-ready PDFs
And other content automation.
Wednesday, 27 March, 2024
11:00 AM CET
How to automate SharePoint document preparation & report generation
And other content automation.
Thursday, March 30, 2023
11:30 AM - 12:00 PM GMT+2
How to automate document preparation & report generation in Veeva with DocShifter
Thursday, 27 April, 2024
11:30 AM CET
How to automate compliant content preparation in OpenText Documentum with DocShifter
Thursday, Aug 29, 2024
6:00 PM GMT+2
How to accelerate content preparation for regulatory submissions: A case study by Pharmalex
How can you automate many of your manual steps in submission content preparation, and how did Pharmalex do it?
Thursday, 21 April, 2022
5:00 PM CET
Translation & Redaction - AI applied in Regulatory Content Preparation
Thursday, Nov 14, 2024
6:00 PM GMT+1