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Regulatory approval of new medical devices: cross sectional study

Regulatory approval of new medical devices: cross sectional study

http://www.wikidata.org/entity/Q24658647

about

Re-evaluation of low intensity pulsed ultrasound in treatment of tibial fractures (TRUST): randomized clinical trial.How much clinical evidence is enough: regulation of medical devices?Types and Distribution of Payments From Industry to Physicians in 2015.Specific barriers to the conduct of randomised clinical trials on medical devices.The role of national registries in improving patient safety for hip and knee replacements.Trends in the diffusion of robotic surgery: A retrospective observational study.Improving patient safety during introduction of novel medical devices through cumulative summation analysis.The regulatory ancestral network of surgical meshes.Robot-assisted stereotactic brain biopsy: systematic review and bibliometric analysis.

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P2860

Regulatory approval of new medical devices: cross sectional study

http://www.wikidata.org/entity/Q24658647

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2016 nî lūn-bûn

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2016 թուականին հրատարակուած գիտական յօդուած

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2016 թվականին հրատարակված գիտական հոդված

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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name

Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Regulatory approval of new medical devices: cross sectional study

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Adam P Marcus

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Christopher J Payne

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Dipankar Nandi

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Hani J Marcus

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Creative Commons Attribution

P2860

Lack of publicly available scientific evidence on the safety and effectiveness of implanted medical devices

Medical device recalls and the FDA approval process

Challenges in evaluating surgical innovation.

Appraisal of evidence base for introduction of new implants in hip and knee replacement: a systematic review of five widely used device technologies

Selective reporting in trials of high risk cardiovascular devices: cross sectional comparison between premarket approval summaries and published reports.

IDEAL framework for surgical innovation 3: randomised controlled trials in the assessment stage and evaluations in the long term study stage.

IDEAL framework for surgical innovation 2: observational studies in the exploration and assessment stages.

IDEAL framework for surgical innovation 1: the idea and development stages.

Translational research: understanding the continuum from bench to bedside.

Making the Leap: the Translation of Innovative Surgical Devices From the Laboratory to the Operating Room.

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10.1136/BMJ.I2587

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353

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Guang-Zhong Yang

Archie Hughes-Hallett

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biomedical investigative technique

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