CMPRO PLM Software Features and Functionality

Learn More About CMPRO

Share CMPRO PLM Software Features & Functionality

Automate business processes & streamline enterprise data management

CMPRO PLM Software Features and Functionality listed below are standard offerings available with CMPRO Enterprise edition for both commercial and government organizations. Need a PDF of the list? A downloadable version is now available. CMPRO PLM Software Features and Functionality Overview - Adobe PDF Download

  • CMPRO Dashboards

    Focused data provides a visual summary of active changes to repository items and where they are in the review process.

  • Drawing and Parts Lists Management

    Centralized repository for managing drawing and parts list data and any corresponding electronic files through revision control.

  • Document Management

    Centralized repository for managing document data and any corresponding electronic files through revision control.

  • Software Management

    Software version tracking and baseline creation from a centralized repository manages software license and location tracking.

  • Configuration Status Accounting

    Both Enterprise and Government approaches used for change control automation and management of system changes.

  • Baselines

    Central control mechanism for maintaining data over time.

  • Product Baselines

    Creates and tracks a combination of released drawings, documents, and software records for a selected top-level assembly or a product structure.

  • Document Baselines

    Creates and tracks the hierarchical document structures that make up processes, procedures, or other documents used for configuration tracking.

  • Software Baselines

    Creates and tracks hierarchical software version structures.

  • Technical Data Package (TDP) System Baseline

    Creates and tracks the relevant technical documentation and change requests/proposals for a system.

  • Contract / DD1423 Tracking

    Oversee contract delivery information including associated contract items, CDRLs (Contract Data Requirements Lists), and associated schedule and delivery records

  • Inventory and Material Management

    Enables inventory operations for multiple warehouses in different geographic locations; provides door-to-door oversight for tracked items and integrates with the As-Built and Work Order Modules.

  • Alterations Management

    Government organization support for field changes, installation tracking, DD1423, and other alterations management tasks.

  • Work Orders

    A workflow-enabled method to oversee building of end-items, assemblies, and buy lists; generate Traveler Packages for recording applicable serial numbers. Track issue orders, instructions, etc.

  • Work Instruction Plans

    Integrates with the Work Order Module to systematically record work to be performed, including required verification checkpoints.

  • Return Material Authorization (RMA)

    Track parts, returns, and swaps.

  • Non-Conformance

    Record, track, report, and process manufactured parts and products that do not meet the specified requirements.

  • As-Built

    Tracks manufactured equipment or systems by platform and location down to a granular, physical level including deployed, fielded products and components with links to periodic maintenance, scheduling, maintenance contracts, and software license tracking.

  • Project Tracker Management

    Track projects, tasks, and action items with links to other workflow forms and actions in CMPRO.

  • System and Subsystem

    Multi-level hierarchy and systems of systems support for organizing product data and facilitating System Baselines.

  • Process Workflow Engine

    Customizable routing system with collaboration features that simplifies electronic forms for change management, process automation, and repository record creation with revision control.

  • Audit Management

    Creates an Audit Master; lists Audit Team, items to be audited, and indicate discrepancy results revealed during the course of the audit. Physical Configuration Audit and Functional Configuration Audit modules included.

  • Report Output

    XLS, CSV, and PDF output, including server generated digitally signed reports.

  • Medical Device and Product Compliance

    Built-in forms, processes, and functionality to support FDA compliance and submission requirements.

  • Corrective and Preventive Action (CAPA) Form

    Workflow-enabled form integrates with other modules to coordinate resulting problem reports, change requests, non-conformances, and real-time status reporting.

  • Design History File

    DHF reporting references records needed to validate approved design plans and fulfill requirements throughout the product lifecycle.

  • Device Master Record

    DMR generated from a system baseline to identify the pertinent documents/procedures/records/specs, etc. and their locations from data managed within centralized repositories.

  • Device History Record

    DHR reporting establishes manufacturing details of a device and its records generated during production, testing, review, inspection, etc. Device data is managed in the As-Built module and links back to DMR data.

Request CMPRO Demo

You may provide as much information as you feel appropriate. We strive to tailor our demos to your business and focus on solving your problems.