ECM for pharma & life sciences

Documented compliance

Provide evidence of your compliance with all regulatory requirements to the authorities, business partners and customers alike.

Efficient production processes

Automate your document-driven production processes and prevent costly errors.

Exceptional product quality

Document quality and ensure that production processes not only run smoothly but also keep on improving.

Marc Volquardsen

What makes Doxis4 different from a conventional DMS platform? Its integrated processes! You have a solution that fully enables you to create documents, manage them via workflows, and document the entire process directly.

Marc Volquardsen, Product Manager for the Doxis4 QM Manual

Prove compliance

Take no risks: From creation to ongoing management, all documents stay fully traceable and under your control. Doxis4 gives you a DMS solution that ensures the validity of your information and simplifies the complex field of compliance.

Expedite research & approval processes

Automate the creation and coordination of patent documents, drug approval paperwork and more and cut down on the time and effort spent on document management.

Breeze through audits

Document ISO standards, the comprehensive protection of sensitive documents, changes to process descriptions and more and quickly provide all information to auditors when required.

Prevent mistakes & enhance quality

Help your employees to follow compliance and QM requirements by making the latest QM manuals available to everyone at all times — and improve the quality of your processes as a result.

Boost research productivity

Collaborate with international research partners, medical professionals and suppliers quickly, transparently and securely in the Doxis4 iRoom. Another benefit: Everyone can work in their local language.

Structure work

Provide employees with all the information they need on studies, research projects, approval procedures and much more in structured digital files that also simplify correct filing.

These pharma & life sciences companies are already working with Doxis4


Show your competitors the door

New drug approvals are at an all-time high, and biosimilars and generics are competing with their branded counterparts. With Doxis4 you accelerate document-driven processes and stay ahead of your competitors when it comes to securing patents and production approvals — without neglecting ever-stricter regulatory obligations. Doxis4 is verifiable: It fully enables you not only to manage documents, but also to demonstrably document quality and compliance and prevent costly errors.

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Quality management with Doxis4

Keep all employees apprised of the latest guidelines, process descriptions and work instructions with Doxis4 — and prove your compliance with quality standards at any time. Read on to find out how the Doxis4 QM manual supports your quality management systems.

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Records management in a regulated environment

Companies in the pharma and life sciences sector are heavily regulated — and a reprieve is not on the horizon. Doxis4 helps you comply with records controls and documentation obligations.

  • Comply with FDA 21 CFR Part 11 on electronic records & signatures
  • Store your records audit compliantly: Doxis4 automatically complies with legal retention periods
  • Manage the data of trial participants in accordance with the EU GDPR — Doxis4 is certified as compliant

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Certified security with Doxis4

Doxis4 is certified to meet numerous domestic, international and sector-specific laws, regulations, norms and standards. Find out here which compliance requirements you can meet with Doxis4.

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Get to know Doxis4 live!

In a live demo or at your place of business.
 

Arrange a Live Demo


How can we help?

Discover with us how Doxis4 can help you meet your goals.

Would you like to learn more about Doxis4 for companies in the pharma & life sciences sector? Schedule your personal live demo of Doxis4 or arrange for us to visit your company to show you its potential live and up close. We look forward to hearing from you!