How CROs & Regulatory Service Providers save time in preparing compliant PDFs
with 3-click automation

Search Results for: Regulatory operations

Creating the right environment for structured and unstructured data to co-exist

There’s a lot of talk about structured information and how it will solve all our problems with regulatory submissions. If you look at initiatives such as IDMP and EMA’s Digital Application Dataset Integration Project (DADI) or further back, FDA’s Structured Product Labeling, there are good examples of health authorities getting at least some information into […]

Creating the right environment for structured and unstructured data to co-exist Read More »

‘Achieve Document Compliance Earlier in Submissions’ — What does this even mean?

If you ever attended one of our webinars, you will have heard us say this a lot. But, what do we actually mean by ‘achieve document compliance earlier’? It is actually a pretty simple concept. Instead of validating the PDF files for compliance with the submission itself (after the draft publishing stage), why not create

‘Achieve Document Compliance Earlier in Submissions’ — What does this even mean? Read More »

Banking & Insurance and Other Regulated Industries

Convert all documents in your Enterprise. Automatically. Centrally. One solution for all your regulatory and other content transformation needs. Finance Insurance Public Sector Other Regulated Industries Trusted by companies of all sizes Committed to delivering the best document conversion/validation software for the regulated enterprise Finance Stay ahead in the competitive banking industry by streamlining document

Banking & Insurance and Other Regulated Industries Read More »

Life Sciences

Accelerate your compliant document preparation. One solution for all your regulatory and other content transformation needs. Pharma & Biotech Medical Devices CRO Services Trusted by life sciences companies of all sizes Committed to delivering the best document conversion/validation software in Life Sciences. Pharma & Biotech Use one solution for all your regulatory and other content

Life Sciences Read More »

3 Click Compliance: What does it mean? How does it work?

Before we introduce what 3 click compliance is, let’s quickly reveal the technology behind it. The technology that makes it possible to significantly speed up and simplify the way you prepare content for submissions today. DocShifter Express. What is DocShifter Express (DS Express)?   DocShifter Express is a browser-based platform that simplifies and streamlines various

3 Click Compliance: What does it mean? How does it work? Read More »

3 ways to automate generation with DocShifter | Automated report publishing | automated report compiling software

3 ways to automate Report Generation with DocShifter

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 these

3 ways to automate Report Generation with DocShifter Read More »

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

Dynamic Scalability in Document Conversion: What is it? Read More »

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

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

What is PDF/A, and how to use the PDF/A file format for digital archiving?

What is the PDF/A format, and how to use the PDF/A format for your Digital Archive

Many of us in business and IT set up and maintain digital archives. Banks, insurance, and healthcare or other regulated industries carry a heavy backlog of archival information going back months or years for thousands of clients.  The Bank of England has a public archive of their work, citing more than 96,000 records just on

What is the PDF/A format, and how to use the PDF/A format for your Digital Archive Read More »

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

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