Medical Device Regulatory Documentation
ISO 13485:2016 Quality Management System Procedures
Management Review Process
Risk Management Process
Internal Audit Process
Human Resources / Training Process
- Human Resources and Training Management Procedure
- Training Record Template
- Training Plan Template
- Organizational Chart Template
- Human Resources Process Package (Procedure + Templates)
Software Validation Procedure
- Computer System Validation Procedure
- Computer System Validation Plan
- Computer System Validation Report
- Computer System Validation Process Full Package (Procedure + Templates)
CAPA Process
- Corrective and Preventive Actions Procedure
- CAPA Template
- Capa Database Template
- CAPA Process Full Package (Procedure + Templates)
Non-Conformity Process
- Non-Conformity Management Procedure
- Non-Conformance Report Template
- Non-Conformance Database Template
- Non-conformity Process Full Package (Procedure + Templates)
Change Management Process
- Change Control Procedure
- Notified Body Change Notification Procedure
- Change Control Template
- Change Control Database Template
- Change Control Process Full Package (Procedure + Templates)
Document Control Process
- Document Control Procedure
- Approval Template Sheet
- Document Master List Template
- Document Control Process Full Package (Procedure + Templates)
Complaint Management Process
- Complaint Management Procedure
- Complaint Handling Template
- Database Customer Complaints
- Database Customer Feedback
- Complaint Management Process Full Package (Procedure + Templates)
Vigilance Reporting Process
- EU Vigilance Reporting Procedure
- US Vigilance Reporting Procedure
- Japan Vigilance Reporting Procedure
- Procedure for Management of Field Actions/Advisory Notices
- Vigilance Reports Database Template
- Vigilance Management Process Full Package
Design Control Process
- Design Control Procedure
- Design and Development Plan Template
- Design Inputs Template
- Design Verification Plan Template
- Design Transfer Checklist
- Traceability Matrix Template
- Design Review Template
- Biological Risk Assessment Template
- Bill of Material Template
- Design History File Index Template
- Device Master Record Index Template
- Design Control Process Full Package (Procedure + Templates)
Supplier Management Process
- Supplier Management Procedure
- Initial Supplier Evaluation Template
- Supplier Monitoring Template
- Supplier List Template
- Supplier Management Process Full Package (Procedure + Templates)
Data Analysis Process
- KPI & Data Analysis Procedure
- KPI List & Data Analysis Template
- Risk Analysis QMS Processes Template
- Data Analysis Management Full Package
Process Validation
- Process Validation Procedure
- IQ Template
- OQ Validation Plan Template
- OQ Validation Report Template
- PQ Validation Plan Template
- PQ Validation Report Template
- Process Validation Full Package
Clinical Evaluation & Investigation Process
- Clinical Investigation Procedure
- Clinical Evaluation Procedure
- Investigator Brochure Template
- Clinical Evaluation Plan Template
- Clinical Evaluation Report Template
- Clinical Evaluation & Investigation Full Package
UDI Management Process
- UDI Management Procedure
- UDI Database Template
- UDI Management Full Package
Post-Market Surveillance Process
Management of Technical Dossier
Customer-Related Process
Labelling Management Process
- Labelling and Management of Translations Procedure
- E-Labelling Management Procedure
- Instructions for Use Template
- Labelling Management Process Full Package
Sterilization Process
- Validation of Ionizing Sterilization Procedure
- Validation of Ethylene Oxide Sterilization Procedure
Infrastructure, Work Environment and Equipment Management
- Infrastructure and Work Environment Procedure
- Control of Equipment Procedure
- Equipment Database Template
Manufacturing Operations
Usability Management
- Usability Procedure
- Usability File Template
- User Related Risk Analysis Template
Management of Communication
Purchase Management
Strategy for Regulatory Compliance
EU MDR 2017/745 Documentation
EU IVDR 2017/746 Documentation
- GSPR Checklist for EU IVDR 2017/746
- Performance Evaluation Plan Template
- PRRC Designation Letter (for IVDR)
- Strategy for Regulatory Compliance (for IVDR)
- Checklist for Technical Documentation According to EU IVDR 2017/746
Technical Documentation Templates
Risk Management
Risk Management Report Template
Design Documentation
Design & Development Plan Template
Design verification Plan Template
Postmarket Surveillance
Postmarket Surveillance Plan Template
Periodic Safety Update Report Template
Postmarket Surveillance Report Template
Usability
Biocompatibility / Clinical
Biological Risk Assessment Template
Investigation Brochure Template
Software Documentation
Software Development Plan Template
Software Architecture Template
Compliance Checklist
Quality Agreements / Contract Templates
- External PPRC Agreement Template
- Quality Agreement (Manufacturer)
- Distributor Quality Agreement
- Importer Quality Agreement