Littérature PubMed
Publications sur les dispositifs médicaux issues de PubMed / NCBI
Regulatory pitfalls and opportunities when repurposing for inhalation therapy.
Lire la suite →Assessment of Obstetric and Gynecologic Food and Drug Administration Device Approvals and Recalls.
Lire la suite →U.S. Food and Drug Administration Precertification Pilot Program for Digital Health Software: Weighing the Benefits and Risks.
Lire la suite →Optimizing outcomes with polymethylmethacrylate fillers.
Lire la suite →Evaluation of Ophthalmic Surgical Instrument Sterility Using Short-Cycle Sterilization for Sequential Same-Day Use.
Lire la suite →Chimie Analytique dans la Science Réglementaire des Dispositifs Médicaux
Lire la suite →Human Subject Protection; Acceptance of Data From Clinical Investigations for Medical Devices. Final rule.
Lire la suite →Comparison of adverse event and device problem rates for transcatheter aortic valve replacement and Mitraclip procedures as reported by the Transcatheter Valve Therapy Registry and the Food and Drug Administration postmarket surveillance data.
Lire la suite →Research Misconduct in FDA-Regulated Clinical Trials: A Cross-sectional Analysis of Warning Letters and Disqualification Proceedings.
Lire la suite →Trials of transvaginal mesh devices for pelvic organ prolapse: a systematic database review of the US FDA approval process.
Lire la suite →Photobiomodulation therapy for androgenetic alopecia: A clinician's guide to home-use devices cleared by the Federal Drug Administration.
Lire la suite →Aucun article correspondant.
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