分类: medical devices

A comparative view on medical device regulations — When West meets East

Written by: Xiaoli Gou and Gert Bos, PhD FRAPS, Qserve Group China

Introduction
Conforming to the local regulatory requirement is essential in introducing medical devices into a market. The medical regulations often permeate throughout the whole product life cycle, from the hatching of a concept, to design and development, to verification and validation, to market approval check, and to post market phase. Having a sound regulatory strategy from the very beginning of the product life cycle and carefully execute the regulatory conformity plan at each stage will ensure the company a competitive advantage in the medical device market.

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首部中国养老产业报告(英文版)问世 A Game-changing Piece of Intelligence for Players in China’s Senior Care Market is Now Available

This report, coming in at over 200 pages, combines 6 months of on-the-ground interviews with key stakeholders driving development at roughly 50 senior living sites and multiple home healthcare businesses. Included in the report are updates on new regulations specific to both senior housing and home healthcare, written by Joe Christian and Michael Qu.

The on-line purchase option is available via our e-commerce store here http://healthintelasia.com/product/china-senior-care-report/

《中国养老产业报告》长达200多页,整合了历经长达6个月、针对近50个养老和居家护理项目的实地考察和深入访谈的成果;其中包括了Joe Christian瞿沁两位律师对养老行业的最新立法动态的详尽分析。

通过以下网址可以购买到本报告: http://healthintelasia.com/product/china-senior-care-report/

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China Releases Measures for Telemedicine Services

At the end of this August, the Ministry of Health and Family Planning (MH&F) promulgated the Measures of Promoting Remote Medical Services among Medical Institutions (Guo Wei Yi Fa (2014) No. 51, “Circular 51”). It is the first detailed policy that regulates the activities of the remote medical services conducted among medical institutions, which is meant to serve as the basic rules of “telemedicine”.

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