Quality & Regulatory Compliance Consultants within the Medical Devices & Diagnostics Industry
Note. We have resources available across mainland Europe
To Request Consulting Support Simply Call +41 (0)78 610 7422
or
email : Barry@Pantheon-consulting.com
EXPERTISE
Quality & Regulatory Compliance Expertise within the Medical Device & Diagnostics Industry
Implementation & Remediation of ISO9001, ISO13485 and 21 CFR part 820 Compliant Quality Systems
Continuous Improvement - Based on Six Sigma & Process Excellence
Electronic Quality System Implementation & Validation
Corporate Quality Policy
Development & Deployment
Quality System Standardization
& Centralization
Embedding Quality Cultures
Project & Change Management
Quality Training Design and Deployment
SERVICES
Expertise Consulting
(face to face or virtual)
Project Managment and/or Project Execution
Strategic Quality Direction & Planning
Quality & Compliance Remediation
Due Diligence Assessments
Root Cause Analysis Workshops
Auditing Services
Quality System Training (live or virtual)
Electronic System Configuration, Implementation & Validation
Regulation & Standards Change
Management (e.g MDR, Brexit)
Product Compliance Assessments
ABOUT US
Pantheon Consulting provides business minded Quality and Compliance support within the highly regulated Medical Device and Diagnostics Industry. Our consultants drive and support initiatives that manage and reduce risk, preserve enterprise value, improve organizational efficiency, and build a culture of Quality and Compliance.
Our retained consultants are highly experienced and have been active in this industry for over 20 years providing guidance and support to global Medical Device Corporations and businesses, helping them to navigate an increasingly complex and volatile regulatory challenges.
CONTACT US
Head Office : +41 (0) 78 610 7422
Montagnier, Valais, Switzerland