Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
[Study on Regulations of Exemption in Medical Device Registration and Approval Process in the United States and China].
Lire la suite →[Analysis on Re-classifcation Management Procedure of Medical Devices in the United States].
Lire la suite →Powered muscle stimulators: an investigation into newly FDA 510(k) approved devices marketed for muscle toning and esthetic benefit.
Lire la suite →United States Food and Drug Administration's 510(k) Pathway: Drawing Implications from the Approvals of Brachytherapy Devices.
Lire la suite →Introduction to Currently Applied Device Pathology.
Lire la suite →Neurological Devices; Reclassification of Electroconvulsive Therapy Devices; Effective Date of Requirement for Premarket Approval for Electroconvulsive Therapy Devices for Certain Specified Intended Uses. Final order.
Lire la suite →Medical Device Classification Procedures: Incorporating Food and Drug Administration Safety and Innovation Act Procedures. Final rule.
Lire la suite →The Importance of Design Validation in Global Health Surgical Innovation.
Lire la suite →Communicating Healthcare Economic and Pre-approval Information With Healthcare Decision-Makers: Opportunities Following the 21st Century Cures Act and FDA Guidance.
Lire la suite →Un aperçu des réglementations internationales sur les dispositifs médicaux : lentilles de contact et solutions d'entretien des lentilles.
Lire la suite →The road to market implantable drug delivery systems: a review on US FDA's regulatory framework and quality control requirements.
Lire la suite →Aucun article correspondant.
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