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Solutions for Pharmaceutical and Life Sciences

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Document Compliance Tools

 

DocsCorp products help professionals in Life Science and Pharmaceutical industries to create and manage the documents they need. Easily assemble and publish paper submissions, white papers, and scientific publications as secure PDF documents complete with headers and footers, links, and bookmarks to help readers navigate through the documents. Assembling electronic copies of studies allows industry members to comply with Environmental Protection Agency (EPA) guidelines on e-submission, as well as comparing PDF draft labels on products before registering the product labels with the EPA.

Products Made for Life Scientists

 

pdfDocs

Managing the paperwork to meet approval deadlines and regulatory rules is a massive undertaking for Life Science and Pharmaceutical companies. pdfDocs' digital workflows make it easier to collate multiple document types from multiple sources into a single PDF that can be easily shared. Often these documents need to be signed with digital signatures and submitted to regulatory bodies electronically. Researchers can do this plus collaborate and review the PDF, adding comments and mark-ups to for all to see. PDFs can be opened and viewed on any platform regardless of whether you have the authoring application or not.

compareDocs

Before submitting documents as part of a clinical trial, Life Science and Pharmaceutical companies need to review them. compareDocs streamlines the review process so that reviewers and researchers who collaborated on the submission documents can compare different versions for changes. Manually comparing documents is a time-consuming process that is prone to error. compareDocs gives Life Science and Pharmaceutical companies a solution that is fast, accurate, and efficient. Moreover, they can be 100% confident in the results.

Pharmaceutical DMScleanDocs

Certainly, Life Science and Pharmaceutical companies would want to protect themselves from inadvertent data breaches given the sensitive information that may be contained in clinical trial documentation. cleanDocs ensures that documents submitted electronically by these companies do not contain hidden metadata, such as comments and Track Changes. It also integrates with email to stop information being sent to the wrong person. cleanDocs gives the control they need over regulatory content.

contentCrawler

Since much of the industries' work is regulated by government and industry bodies, Life Science and Pharmaceutical companies need to be able to produce documents on demand. Failure to do so can lead to serious fines and penalties. contentCrawler ensures all documents are 100% searchable and retrievable, reducing the risk of non-compliance or lost productivity looking for lost or misfiled documents.

Looking for more than 20 licenses? Contact us to know more.

Pricing

 

Industry Resources

 

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Press Release

Latest compareDocs Release Expands Document Comparison

Latest compareDocs Release Expands Document Comparison to Include Comparing Snippets of Text or Code for Differences

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Case Study

contentCrawler shines light on missing document

contentCrawler empowers Electricity Authority to find “invisible” documents in their DMS

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Industry Guide

This industry guide looks at new data protection regulations in places like Europe, America, and Australia, and how to protect against the number one cause of data breaches.

Reviewing your data protection strategy in 2018

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Blog Post

By Ben Mitchell, Vice President of DocsCorp Europe

Why Accidental Leaks Should Have You Worried

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Case Study

contentCrawler helps find critical documents and drawings, ending engineers’ frustration with DMS

PTTEP Australasia ends missing search data frustration by implementing contentCrawler

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Blog Post

The latest version of pdfDocs Binder is designed to work the way you do.

New Feature: Add custom metadata to electronic binders with pdfDocs

The only product on the market that combines metadata cleaning and recipient checking

Learn More

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