We’ve created a checklist to help you optimize your PDF documents for eCTD submissions. Enter your email below and we’ll send it directly to you. Pharmaceutical and biotechnology companies spend a lot of effort in the R&D process of a new medicine or a product. As every stage must be properly documented, a typical R&D […]
Free FDA PDF Specifications Checklist Read More »
1. For the viewer, a report is just a series of PDF files. But for the author(s), a report means a lot of hard (manual) work and effort. With so many manual tasks involved, the report creation process is typically very time-consuming and prone to errors. Adopting an automated PDF report generation software significantly streamlines
3 ways to automate Report Generation with DocShifter Read More »
Introduction: “Converting to PDF is easy, and everyone does that. The problem is us spending hours and hours of time on editing PDFs with Acrobat, or other desktop tools. Especially not knowing what was wrong with the PDFs. And that is what DocShifter does for us.: fixing all our PDFs automatically, or at least telling
Win-win for partners, customers and end-users “We are very pleased to strengthen our global presence through this valuable partnership” said Geert Van Peteghem, CEO of DocShifter. “The Indian economy is growing at a rapid pace. And India has rapidly become an important global player in the pharmaceutical industry, where most of our customers operate.
Expansion to India! Exciting times ahead. (Press Release) Read More »
Continuing the LinkedIn Live thought leadership series with Aki Yamaguchi from LORENZ Life Sciences Group. During this LinkedIn live session, Mr. Yamaguchi and Paul Ireland will discuss the global aspects and the future direction of the electronic common technical document. What can you expect to see in the video? What is/was the main purpose for
eCTD Global Aspects and Future Directions (LinkedIn Live Session) Read More »
![[Webinar Summary] How to automate PDF rendering with DocShifter featured image](https://test.docshifter.com/wp-content/uploads/2023/06/featured-image-1-6489aedde2b47-1024x576.webp)
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 »
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
Dynamic Scalability in Document Conversion: What is it? What are the benefits? 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 »
With so many mature and emerging digital technologies, and no end of interesting use cases in Regulatory, how do we decide which ones are worth it? And most importantly, who pays vs who benefits? This was the topic during our third LinkedIn live session with John Cogan. For those who missed the live event, the
The Economics of Technology Innovation in Regulatory Read More »
15 years of experience in automating, simplifying and speeding up document conversion. For all regulated industries. Rated 5 stars on Gartner’s Capterra platform.
