Литература PubMed
Публикации о медицинских изделиях из PubMed / NCBI
[Study on Regulations of Exemption in Medical Device Registration and Approval Process in the United States and China].
Читать далее →[Analysis on Re-classifcation Management Procedure of Medical Devices in the United States].
Читать далее →Powered muscle stimulators: an investigation into newly FDA 510(k) approved devices marketed for muscle toning and esthetic benefit.
Читать далее →United States Food and Drug Administration's 510(k) Pathway: Drawing Implications from the Approvals of Brachytherapy Devices.
Читать далее →Introduction to Currently Applied Device Pathology.
Читать далее →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.
Читать далее →Medical Device Classification Procedures: Incorporating Food and Drug Administration Safety and Innovation Act Procedures. Final rule.
Читать далее →The Importance of Design Validation in Global Health Surgical Innovation.
Читать далее →Communicating Healthcare Economic and Pre-approval Information With Healthcare Decision-Makers: Opportunities Following the 21st Century Cures Act and FDA Guidance.
Читать далее →Обзор международных регуляций медицинского оборудования: контактные линзы и растворы для ухода за линзами.
Читать далее →The road to market implantable drug delivery systems: a review on US FDA's regulatory framework and quality control requirements.
Читать далее →Подходящих статей не найдено.
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