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1. Do not wait until the last minute to resolve content-related issues 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 at the end of this timeframe. Documents are typically only checked for compliance either just prior to […]
[Webinar Summary] How to automate PDF rendering with DocShifter Read More »
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
Accelerating submission-ready PDF rendering. A case story by PharmaLex. Read More »
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 at the end of this timeframe. Documents are typically only checked for
5 ways to automate your submission content preparation in Veeva with DocShifter Read More »
PharmaLex, a leading provider of specialized services for the pharmaceutical, biotech and medical device industries, chose DocShifter to simplify and accelerate the generation of compliant, submission-ready PDF documents for their 1000’s of clients worldwide. PharmaLex’s services include document pre-publishing and regulatory submission publishing, therefore managing large numbers of documents in different formats and differing
15 years of experience in automating, simplifying and speeding up document conversion. For all regulated industries. Rated 5 stars on Gartner’s Capterra platform.
