Web-based Quality Management Across the Enterprise

Industry

Aerospace

Automotive

Construction

Environment

Healthcare

Semiconductor

Telecommunications

Transportation

Healthcare

Document Pro is a document management software system that will enable pharmaceutical, biotechnology, medical device and other FDA-regulated industries to comply with 21 CFR Part 11 and meet FDA GMP, GLP and GCP requirements. Our document control and quality management solutions are helping companies simplify Part 11compliance.

How can the EwQMS® System assist you in the management of ISO 9001:2000 / CFR Part 11?

Implementing electronic signatures and electronic records with Document Pro as specified by 21 CFR Part 11

• Document Pro allows you to search and find documents in a fraction of the time currently required.
• Document Pro helps you to avoid the costly time delays associated with lengthy approval cycles.
• Document Pro prepares you for FDA inspections. 

News Headlines

AIAG has released the 4th Edition FMEA Reference Manual.
To help you get up-to-date with the changes made in the latest revision, Omnex conducted a two separate webinars on August 5 and October 16, 2008. A recording of these webinars and/or a hardcopy of the material are available for purchase. Click here for more information.

Multimedia Overview

EwQMS® Multimedia Overview

Training & Consulting

Omnex Training & Consulting