• Periodic Safety Update Reports (PSURs)

• Data gathering and Analysis

• Trending

• Competitor Analysis

• Proactive Surveys

• Benefit / Risk Analysis

• Summary of Safety and Clinical Performance


• Clinical Investigation and Reporting

• State-of-art justification

• Data analysis

• Literature review

• Benefit / Risk Analysis

• Update of IFUs and regulatory files


• Maintenance and Compliance updates

• FDA 21 CFR Part 820, EU MDR 2017/745

• ISO 13485, ISO 14971, ISO 9000

• Efficiency / Productivity Improvements

• Simplification

• Waste eliminations

• Organization / Structurization


• Rapid updates and simplification of risk files

• Risk assessments and mitigations


• Health Hazard Evaluations

• Product / Process Root Cause Analysis

• CAPAs

• Global Field Actions

• Recalls / Services

• Safety notices

• Coordination with authorities


• Complete Process Development and Deployment

• Medical Device Reporting

• Complaint Investigations and Field Investigations


• CAPA management (Corrective and Preventive Actions)

• Non-conformance material handling

• Rapid production recovery and supply chain continuation


• Analysis and rapid recovery of global supply chains issues

• Immediate organizing multi-functional and globally disperse teams/functions