Basic info
Industry
medical equipment manufacturing
Sectors
High Tech Device Design
Contract Packaging
Quality Management System Implementation/Maintenance
Regulatory Audit
FDA 510(k) Regulatory Pathway
Regulatory Tech Filing
CAPA Consulting
Medical Device Regulation
Human Factors Design
Contract Manufacturing
Medical Device Design
CE Mark Certification
Catheter Design
Prototype Production
Plastic Injection Molding
Health Care
Contract Sterilization
ISO 13485:2016 Certified
Manufacturing
Ethylene Oxide Sterilization
Information Technology
Clinical Evaluation Reports
Verification and Validation Testing
Date founded
2009