CMPRO PLM Software – Standard Functionality
Product Lifecycle Management Software Designed to Automate Business Processes & Streamline Enterprise Data Management
Centralized Repositories, Integrated Modules and Dashboard Systems
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.
Centralized repository for managing document data and any corresponding electronic files through revision control.
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.
Central control mechanism for maintaining data over time.
Creates and tracks a combination of released drawings, documents, and software records for a selected top-level assembly or a product structure.
Creates and tracks the hierarchical document structures that make up processes, procedures, or other documents used for configuration tracking.
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.
Government organization support for field changes, installation tracking, DD1423, and other alterations management tasks.
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.
Record, track, report, and process manufactured parts and products that do not meet the specified requirements.
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.
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.
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.