加拿大对避孕器具的管制。

Contraceptive delivery systems Pub Date : 1984-01-01
M S Smith
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引用次数: 0

摘要

口服避孕药(OCs)、宫内节育器、人工流产技术和腹腔镜手术的广泛使用和相关技术的发展导致了需要政府控制的危害。介绍了由医疗器械局负责的避孕器具的目标和管理方面。制定自愿和管制两方面的质量标准,以及对避孕器具实行上市后管制的重要性,都是最近的发展,旨在确保改善加拿大公众的健康。新的和正在发展的避孕装置技术可能对加拿大公众的健康和福祉产生深远的影响。确保避孕器具的安全性和有效性的挑战必须通过受影响患者的沟通来更好地解决。与病人接触的内科医生和其他专职医疗人员必须对病人的关切敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Canadian regulation of contraceptive devices.

Widespread use and technical developments associated with oral contraceptives (OCs), IUDs, techniques involved with abortion, and laparoscopy have resulted in hazards which require governmental control. The objectives and regulatory aspects of contraceptive devices undertaken by the Bureau of Medical Devices is described. The development of quality standards, both voluntary and regulatory, and the importance of postmarket controls for contraceptive devices are recent developments designed to ensure improvement in the health of the Canadian public. New and developing contraceptive device technology may have profound effects on the health and wellbeing of the Canadian public. The challenge of ensuring the safety and efficacy of contraceptive devices must be better met by communication from those patients who are affected. Physician and other allied health professionals who interface with the patient must be sensitive to the concerns of the patients.

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