Posts in: 四月, 2017

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

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

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.


全国开展养老院服务质量建设专项行动A Nation-wide Special Action for Nursing Homes Services Quality Construction is Rolling Out


In order to intensively deploy President Xi Jinping’s advocate for “carrying out quality improvements activities” at the Central Economic Work Conference and the important speech spirits of improving the nursing homes services quality (NHSQ) at the 14th Central Finance Leading Group Meeting, to strengthen the quality supervision of nursing homes, departments of Ministry of Civil Affairs (MCA)、Ministry of Public Security (MPS)、National Health and Family Planning Commission (NHFPC)、General Administration of Quality Supervision, Inspection and Quarantine (AQSIQ)、Standardization Administration (SA)、National Aging Office (NAO) decide to carry out special action of NHSQ construction nationwide.