2. Electronic & High Tech Solution (Focus)
Medical Device Solution (Short introduction)
Minerva Group
3. Product Data Management
Test Data
Mechanical Designs Electronic Schematics
Components
Marketing Literature
900
800
700
600_1
Logical_01
Physical_01
Fab_01
11-1111-01
11-222-01
11-333-01
600_2 SYM_CAP01 PCB Layouts
Bills of Material
Documentation
Specifications Software
4. Virtual Value Chain Evolution Drives Complexity
Customers
Service
Engineering
Design
Partners
Marketing
Manufacturing
Quality Service
Procurement
Partners
Suppliers
Mfg Partners
Government
and
Suppliers’ Standards
Suppliers
5. EH&T Solution Overview
Network Drives
CAD
• Easy Grant Access
• Faster than CAD integration • Defined collaboration
• Import to ECO with differences • Enchanced Parts Management processes
• Maintain history • Extended Lifecycle Management • Participate in ECO
• No manual error • Minor Revision • Create ECR
• Advanced Best Practice Change Management • Easy extract of information
• Intelligent Workflow choice based on business logic
6. Minerva in Action
Business Profile Business Case
Company: Challenge:
• Efficiency, traceability, control and visibility into product
CPAC AB
documentation and associated processes
• HQ S. • Multiple data islands combined with manual processes for
Products: handling product documentation, collaboration, change
management, release management and more.
Control Systems
Solution:
Industry:
• PLM Solution setup specific for Electronics and
Electronics & High-tech high-Tech with Mechanics, electronics, and software.
Implementation: • Change Management
15 Days • Collaboration with external partners
7. Extended into Medical Device industry solution
CAPA Process
-Problem Reports
-Quality Service Request (root
DHF Quality System cause analysis)
-Phase Gate & -Change Orders
-Design Review Quality
Corrective &
Corrective & System
Preventive
Preventive
Actions
Actions
Regulation
Design
Design Controls
Production &
Controls Process Controls
Management
Material
Material Equipment & Regulatory
Controls
Controls Facility Controls Audit
-Approved Records,
Records,
Maufacturers/ Documents & &
Documents, i.e. FDA CFR 820
Change Control
-Vendors Change Controls
-NCMR Product Record
DHF DMR SOPs Process history/evidence
-Documents
Personnel Skills Quality Audits . . .
7
8. Minerva Products
• Industry solution for EHT & Med Dev
• Tools
– Minerva Import
– Minerva Special Permission Manager
– PDX Export
– Office Connector
– ConfInnovator
• See more at www.minerva-plm.com
• Come talk to me in the break
