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PharmaLex speeds up their customers' submissions and content preparation thanks to DocShifter's automated submission-ready PDF conversion capabilities

Pharma time-to-market reduced thanks to more efficient submission document publishing services

  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 […]

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How to design an enterprise file conversion platform?

How to design or implement an enterprise file conversion platform?

What is enterprise file conversion? What does it mean? Enterprises or businesses deal with a lot of documents, in multiple formats. Word, Excel, PowerPoint, PDF, PDF/A, scanned images, JPEG, TIFF, audio and video files, XML, HTML, e-mail files and many more. All these files need to be converted for many reasons: standardization, digital archiving, customer

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How to reduce content creation issues in regulatory submissions?

How to reduce regulatory content creation issues? 4 tips.

Life Sciences organisations are required to create huge quantities of documentation to support the marketing of their products around the world. Industry standards have been put in place to ensure that Global Health Authorities receive content in a manner that simplifies the review and approval process of new medicines or devices. These guidelines do provide

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How to select a document conversion software for your enterprise?

Document conversion software for enterprises: which solution should I choose?

What is enterprise document conversion, and how does a document conversion software impact your business? Enterprise document conversion is the process of converting different digital file formats into other formats so that they can be used in various business processes (standardization, customer communication, digital archiving,  sharing and collaboration, etc.) and applications (CRM, ERP systems, etc.).

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6 reasons to rethink your document rendering / document conversion software - blogpost by DocShifter

6 Rocking Reasons to Rethink Document Rendering

We have been rendering various documents into a unified format such as PDF for many years now. For many reasons: ease of use, accessibility, a wide range of functionalities and many more.  In knowledge-driven industries, the need for standardization is often forced by regulators. For example, in Life Sciences, the introduction of the electronic Common

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3 tips to save time and reduce risks in regulatory submissions in Life Sciences

3 tips to save time and reduce risk in regulatory submissions

How can you speed up the process of getting your medicinal products approved by health authorities? At the same time, how can you reduce the risk of submitting PDFs that are not complying with technical requirements in your regulatory submissions? Our tips will help you streamline the whole regulatory submission process. For Life Sciences companies,

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How do you deal with track changes in Microsoft Word when converting to PDF?

Track changes and comments don’t look consistent when you convert Microsoft Word documents to PDF?

Are you having trouble converting Microsoft Word documents containing track changes and comments to PDF? Creating consistent output when converting MS Word documents containing track changes into PDF is a big challenge. With multiple reviewers and authors working on the same document, each with their styling, getting this consistency is almost an impossible mission.  Do

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What is the role of data in regulatory submissions? Is the role of data, taking over the role of PDF in electronic submissions in life sciences?

Is data taking over the role of PDF in eCTD submissions?

The Life Sciences industry is dedicated to protecting the health of millions of individuals worldwide. The industry is also looking to improve their lives with affordable and easily accessible medicinal products. Patient and patient safety always comes first, which is why the process of bringing a drug to the market takes many years (from 8

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Refusal to file (RTF) in life sciences: What does it mean and how to reduce risk of RTF in regulatory submissions?

Refusal to File (RTF) and how modern rendering can reduce non-compliance risk

Bringing a new medicine or a product to the market is a complex process that typically takes from 8 to 14 years. Although this process may vary from one Health Authority (HA) to another, there are some general stages that the medicine must go through before it can be safely distributed to patients. It starts

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