PubMed 문헌
PubMed / NCBI의 의료기기 관련 문헌
[Study on Regulations of Exemption in Medical Device Registration and Approval Process in the United States and China].
더 읽기 →[Analysis on Re-classifcation Management Procedure of Medical Devices in the United States].
더 읽기 →Powered muscle stimulators: an investigation into newly FDA 510(k) approved devices marketed for muscle toning and esthetic benefit.
더 읽기 →United States Food and Drug Administration's 510(k) Pathway: Drawing Implications from the Approvals of Brachytherapy Devices.
더 읽기 →Introduction to Currently Applied Device Pathology.
더 읽기 →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.
더 읽기 →Medical Device Classification Procedures: Incorporating Food and Drug Administration Safety and Innovation Act Procedures. Final rule.
더 읽기 →The Importance of Design Validation in Global Health Surgical Innovation.
더 읽기 →Communicating Healthcare Economic and Pre-approval Information With Healthcare Decision-Makers: Opportunities Following the 21st Century Cures Act and FDA Guidance.
더 읽기 →국제 의료 장비 규제: 콘택트 렌즈와 렌즈 관리 솔루션에 대한 리뷰.
더 읽기 →The road to market implantable drug delivery systems: a review on US FDA's regulatory framework and quality control requirements.
더 읽기 →일치하는 논문이 없습니다.
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