痛恨
发表于 2025-3-23 12:20:41
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insolence
发表于 2025-3-23 16:18:35
Hideo Tanaka,Kazutomi Sugihara,Yutaka Maedae been thoughtful design and engineering, carefully controlled manufacturing specifications, thorough laboratory pulse-duplicator and wear testing, animal implantation, and limited initial clinical use with thorough and complete hemodynamic and clinical follow-up.
圆柱
发表于 2025-3-23 19:27:06
Studies in Fuzziness and Soft Computinge lengthy history and, as such, has been frequently—and at times inappropriately—used as a template for establishing standards for the conduct of orthopedic research. Both, however, share certain basic elements that are central to realizing good clinical research.
Coterminous
发表于 2025-3-24 01:53:49
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肉体
发表于 2025-3-24 04:22:42
Categorical Innovations for Rough Setsd and Drug Administration (FDA). However, this categorization may be questionable. Other regulatory authorities consider hyaluronic acid products as drugs because the mechanism of action appears to go beyond the mere physical function of replacing abnormal synovial fluid (“viscosupplementation”).
变形词
发表于 2025-3-24 10:02:56
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Germinate
发表于 2025-3-24 14:27:39
Hongyuan Shen,Shuren Yang,Jianxun Liuperformance of marketed products may be misleading if not done appropriately. Clinically based postmarket surveillance can reveal the true actuarial survival of a device and the clinical mode of failure. Analysis of returned products may be required to understand the details of failure mechanisms ..
chronicle
发表于 2025-3-24 15:13:54
device trials. A few years ago, device developers would look askance if one told them that medical device trials and drug trials should have the same stan dards. Today, such a statement does not seem as outrageous, although there is still a large gap in the design of trials and number oftrials cond
的染料
发表于 2025-3-24 22:19:51
Rough Set Methods and Applicationsed effect. As defined in the US Food, Drug and Cosmetic Act, the term medical device.This broad definition of medical devices encompasses literally tens of thousands of different types of health-care products, including in vitro diagnostics.
conjunctiva
发表于 2025-3-25 02:01:03
Jerzy W. Grzymala-Busse,Rachel L. Freeman chapter will provide information on FDA regulatory requirements for controlled clinical investigations of medical devices and diagnostics, including who must conduct a clinical trial, the submissions required, and the procedures that must be followed.