PLMplus for Medical Devices

PLMplus for Medical Devices is a combination of a Product Lifecycle Management System, with deeply embedded Quality Management features, typically found only in QMS systems. 

PLMplus is specifically designed to solve the needs of companies that are developing  products that need to meet compliance standards such as FDA 21 CFR Part 11.  If your company is in that group, it is likely that you have to face all the tough development challenges faced by non-medical companies, but you also have to ensure high quality and compliance at every step of the process.  PLMplus for Medical Devices solves that pain, it helps you accelerate your product development cycle while ensuring that you remain compliant.

• Medical & FDA compliance
• Design control management
• CAPA management
• Internal audit
• Non conforming material
• Audit trail & signatures
• Approved vendor list
• Document control

• Engineering
• Item management
• BOM management
• Change management (ECOs / Workflows)
• Document management
• Distributed office collaboration
• Supplier collaboration
• Reporting & Analytics
• Realtime visibility into development progress
• Automated key performance indicators
• Measure & improve performance
• Infrastructure
• On-Demand software
• Pay for the service only as long as you use it, on a price / user / month basis. 
• System designed to used without formal training
• Preconfigured system & database complete with industry best practices