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

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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Dynamic Scalability in Document Conversion: What is it?

In today’s digital age, organizations are generating and handling an unprecedented amount of digital documents in various file formats. From invoices and reports to contracts and customer records, the need to convert documents from one format to another is an everyday requirement. However, managing the conversion process efficiently is challenging, especially when faced with fluctuating

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Accelerating submission-ready PDF rendering. A case story by PharmaLex, a leading solution provider for pharma & biotech.

Accelerating submission-ready PDF rendering. A case story by PharmaLex.

PharmaLex provides document pre-publishing and regulatory submission publishing services for multiple clients and therefore receives large numbers of documents in a variety of formats and quality. The documents are a mixture of Administrative (Cover Letter, Application form), Summaries, Quality, Non-Clinical and Clinical content. PharmaLex was previously using licensed PDF plug-in tools to prepare content for

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

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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5 ways to automate your submission content preparation in Veeva with DocShifter - Accelerate your regulatory submissions and reduce time to market

5 ways to automate your submission content preparation in Veeva with DocShifter

Here are 5 ways to automate submission content preparation in Veeva with DocShifter 1. Achieve document compliance earlier in your submission process when using DocShifter with Veeva (or any other repository) A typical drug development process takes from 5 and 15 years, and documentation is created every step of the way. Marketing Authorisation submissions are compiled

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How to automate SharePoint document preparation & report generation

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)

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 +

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

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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