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Practical example of report compilation: Automation with DocShifter. What, how and benefits (with a practical demo) Webinar banner

Report Generation Automation with DocShifter (with a practical demo)

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Are you creating your reports manually today? Or perhaps using complex submission publishing tools to build your reports? Investigational medicinal product dossiers (IMPD), clinical study reports (CSR), annual reports, training manuals, standard operating procedures (SOP) and even full 510k & PMA submissions could all benefit from a tool designed specifically for their creation. ​Merging multiple […]

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How to automate PDF rendering for global submissions with DocShifter website webinar banner

How to automate PDF rendering for global submissions with DocShifter (with a practical demo)

Leave a Comment / Past Webinars, Automated Report Level Publishing Resource 1, Submission Ready Pdf Resource 1 /

The process of preparing content for submissions is very time-consuming and financially burdensome ​Using multiple desktop tools, and spending hours or even days, manually editing PDFs to meet the FDA, EMA, PMDA, etc. requirements  ​Manually checking and fixing thousands of PDF files for submission readiness ​Re-working external content to ensure document compliance ​Validating content too late, and the risk of missing submission deadlines ​Authors

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How to automate document preparation & report generation in Veeva with DocShifter

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Are you using Veeva to store and manage your submission content? ​The automation of regulatory content does not need to stop there. ​Combined with the power of DocShifter, we can take automation to the next level. So you can focus on the content. ​How will this powerful combination help you save time with the following?

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How to automate SharePoint document preparation & report generation

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Are you using Microsoft SharePoint to store and manage your submission content? ​​The automation of regulatory content does not need to stop there. ​​Combined with the power of DocShifter, we can take automation to the next level. So you can focus on the content. ​​How will this powerful combination help you save time with the

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How to save time by fully automating your report level publishing and report generation needs webinar header

How to simultaneously render compliant PDFs for your global submissions (including a 15 minute practical demo)

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Are you struggling to produce PDFs that meet the requirements of different regulatory agencies around the world? Do you find yourself spending hours, or even days, manually editing PDFs to meet the FDA, EMA, PMDA, etc. requirements? Today, this process does not have to be this complex and difficult. Join us in this webinar +

How to simultaneously render compliant PDFs for your global submissions (including a 15 minute practical demo) Read More »

How to save time by fully automating your report level publishing and report generation needs webinar header

DIA RSIDM 2022 Abstract – Lessons Learned on Document Preparation in Life Sciences

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Regulatory submissions are one of the most critical milestones for Life Sciences organizations. Submitting on time & in full compliance with regulatory agencies’ requirements, remains a challenge. Life Sciences organizations adopt cutting-edge technology, but the technology alone doesn’t guarantee compliance & that timelines are met. Efficient processes combined with technology does.   This webinar outlines how

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Innovative Approaches in Modern Rendering. Reduce Risk, Time and Effort to Ensure HA Compliance

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December 22, 2020Creating compliant submission-ready PDFs for inclusion in dossiers has proven to be time-consuming, expensive and complex. In this session we share how your peers use modern rendering technology to speed up, reduce the cost of and simplify this process. Our special thanks to the Lorenz team for having us at their Lorenz Connect

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Generate compliant PDFs for multiple HAs automatically BEFORE publishing eCTD leafs

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May 26, 2021Are you getting ready for your next submission? And interested to simplify and speed up submission content creation? Manipulating and finalizing PDFs using desktop tools is a manual task: embedding fonts, checking hyperlinks, adding ToCs and making sure they comply with HA requirements. And repeating this for 100.000s of documents. All this manual

Generate compliant PDFs for multiple HAs automatically BEFORE publishing eCTD leafs Read More »

The secrets to a successful enterprise (PDF) conversion platform webinar header

The secrets to a successful enterprise (PDF) conversion platform

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September 5, 2021For 40 years now, we have been creating content digitally. Documents, spreadsheets, databases, presentations, videos, audio files… We created 2.5 quintillion data bytes every day in 2018. That number is only increasing exponentially and expected to reach 175 zettabytes of data in the global datasphere by 2025. Much of this content will need

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15 years of experience in automating, simplifying and speeding up document conversion. For all regulated industries. Rated 5 stars on Gartner’s Capterra platform.

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