CMPRO PLM Software Features and Functionality

Automate business processes & streamline enterprise data management

• 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.