Regulation of medical devices in the United States and European union

Keyphrases

• United States 100%
• Medical Devices 100%
• European Union 100%
• Disease Diagnosis 33%
• High Risk 33%
• Device-independent 33%
• Disease Management 33%
• One-generation 33%
• Heart Valve 33%
• European Patients 33%
• Postmarket 33%
• Quality Assurance Program 33%
• Intraocular Lens Implant 33%
• Coronary Stent 33%
• European Commission 33%
• Reasonable Assurance 33%
• Medical Device Amendments 33%
• High Risk Medical Device 33%

Nursing and Health Professions

• Medical Device 100%
• Food and Drug Administration 60%
• Practice Guideline 20%
• Disease Management 20%
• Quality Control 20%
• Intraocular Lens 20%
• Joint Prosthesis 20%
• Coronary Stent 20%

Pharmacology, Toxicology and Pharmaceutical Science

• Diseases 100%