Life Sciences & Medical Devices
Life sciences, pharmaceutical, and bioprocessing manufacturers.
Medical device companies seeking practical quality and compliance solutions
NobleQ Consulting supports Life Sciences and Medical Device manufacturers in building compliant, high-performing quality systems across FDA- and ISO-regulated environments.
Specialized services include:
• Audit Readiness & Regulatory Compliance Support
• Quality Management System (ISO 13485, ISO 9001) Setup & Deployment
• CAPA System Implementation & Internal Audit Training
• Risk Management (DFMEA / PFMEA) and Process Validation
• GMP Compliance & Environmental Monitoring Program Design