Document Management Software | DocPro

Document Pro | Document Version Control Software

Document Pro is a single repository to manage all your business documents and records. You can monitor employee access, document revisions, change requests, and approvals through an online platform. Documents can be customized into infinite number of levels and folders per structural requirements. The system follows a pre-programmed base structure in which; Level 1 is for Quality Manual, Level 2 for Processes, and Levels 3 and 4 for Work Instructions and Checklists, respectively. Especially powerful for integrated management systems!

Document Pro software is compliant with the following standards:

ISO 9001:2015
IATF 16949
Aerospace AS9145
FDA CFR 21 Part 11
ISO 13485
ISO 14001
ISO 45001
FSSC 22000

Request for Demo

Features and Benefits (Document Management Software - Document Pro)

Comprehensive Integrated Document Management System

Single source of truth for documents within the Organization, including Management Systems documents like documents, forms, and records.
Facilitates Integrated Document Management systems for Organizations that are juggling multiple standards.

Multiple level(s) of documentation structure

Model your current management system within DocumentPro, with minimal impact to current disciplines.

Organize, Share, Track, Review and Approve Documents

Manage documents from a single system of record to complete document lifecycle.

Search Effectively

Search titles, and even embedded content, to retrieve documents.

Approval Workflows

Automated Approval workflows to help effective Document approval process.

Multi-module documentation management

Acts as a single repository for reports/documents published from other EwQIMS modules.

Document Tags

Create searchable document tags to search, sort, and group documents by related keywords.

Online Documentation:

Create Process Maps, Procedures using Online forms; link these documents with Work Instructions and Checklist. Create documents easily without MS Word/PDF.

Case Study & White papers

Digitalization of FMEA, Control Plan, and other APQP/PPAP documents using EwQIMS - Enterprise FMEA Solution

A global leader in the development and production of high-precision bearings for aerospace, defense, medical, dental, and high-tech...

White Paper: Best Auditing Practices using Software

Enterprise today is juggling many standards. An audit tells an organization whether it is adhering to statutory and regulatory requirements and established objectives.

Focus on APQP/PPAP Documentation

The global growth objectives of the customer were hampered by the spreadsheets and silo-based client-server applications that lacked standardization as it is with 75% of the automotive supply base.

Enterprise Quality Management System Software

Digital Transformation of Enterprise Quality

This Automotive Tier-1 wiring harness company was established in 1941 and is one of the world’s leading independent
automotive component manufacturers.

Digitalization of PPAP Documentation Solution Case Study

A global Aerospace organization with several plants in product and process development had challenges with centrally managing all design/process artifacts that were created

The New AIAG-VDA FMEA First Edition White Paper

The AIAG-VDA FMEA Handbook, released in June 2019 has begun to gain popularity in the Automotive Industry globally. Both US and European OEMs have started to require the use

Virtual Supplier Quality Management Solution powered by AI

Managing suppliers virtually with an Enterprise supplier quality solution is a requirement in today’s environment. A “new normal” is emerging where the ability

Who We Work With

100,000+ globally has embraced Digitalization of Quality

Insights

From Percent Rejects to Parts Per Billion Moving Towards Zero Defects

Quality improvement and defect prevention start with a disciplined, new-product development process that includes phase gates...

Empower Your Team With Enterprise APQP Solution

APQP (Advanced Product Quality Planning) is a proven methodology used to develop products in a variety of industries.

Develop AIAG & VDA FMEAs with 50% Effort

Watch the webinar recording to understand all about AIAG-VDA-FMEA and how to develop with-50-percent-Effort...

Implementing A Zero Defects Program

This webinar is dedicated to exploring the ways in which APQP incorporates and uses lessons from the past, using break-through product and process design...

Let's Connect

Tell us how we can help you in your Digitalization Journey.

+1 734-761-4940

[email protected]

Omnex Inc., is committed to protecting and respecting your privacy. We will only use your information to administer your account and to provide the products and services you requested from us. From time to time, we will contact you about our products and services, as well as other content that may be of interest to you. You can unsubscribe from these communications at any time, please review our Privacy Policy.

Submit