Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Pei-Weng Tu"'
Publikováno v:
The International Journal of Advanced Manufacturing Technology. 109:2421-2429
In this study, two selective metal fusion additive manufacturing (AM) technologies, electron-beam melting (EBM) and selective laser melting (SLM), were used to fabricate Ti6Al4V test specimens for a comprehensive evaluation, including physical-chemic
Autor:
Pei-Weng Tu
Publikováno v:
Medical Affairs ISBN: 9781003207696
Medical Affairs
Medical Affairs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c97ae8688ee1a7aa4efc9d75ab63249d
https://doi.org/10.1201/9781003207696-39
https://doi.org/10.1201/9781003207696-39
Autor:
Yin-Ting Fan, Jin-Yu Lee, Yu-Che Cheng, Hsin-Hui Lin, Chia-Hung Chien, Pei-Weng Tu, Hui-Wen Chung
Publikováno v:
Journal of the Chinese Medical Association; Nov2022, Vol. 85 Issue 11, p1038-1043, 6p
Autor:
Ching Chou, Yung-Hsin Chen, Tsair Kao, Mei-Fen Chen, Kang-Ping Lin, Chia-Hung Chien, Cheng-Ning Wu, Pei-Weng Tu, Cheng-Lun Tsai
Publikováno v:
Journal of Medical and Biological Engineering. 40:101-111
The aim of this study is to examine how aesthetic devices are defined and managed. Regulation discrepancies between clinical use and home use in four regions are also described. The official websites and databases of US, European, Chinese, and Taiwan
Autor:
Ching Chou, Yu-Wen Huang, Pei-Weng Tu, Cheng-Ning Wu, Kang-Ping Lin, Chia-Hung Chien, Yung-Hsin Chen, Mei-Fen Chen, Tsair Kao, Cheng-Lun Tsai
Publikováno v:
Journal of Medical and Biological Engineering
The aim of this study was to establish a web-based platform for exchanging medical device management and maintenance experiences to enhance the professional competency of clinical engineers (CEs), which ensures the quality of medical devices and incr
Publikováno v:
Therapeutic Innovation & Regulatory Science. 52:62-69
The medical device industry is an industry dealing with multiple types of products covering a wide range of applications. As the safety and effectiveness of medical devices are vital to human health, the products must be managed by strict regulations
Publikováno v:
Expert Review of Medical Devices. 14:285-296
Introduction: In Taiwan, In Vitro Diagnostic Medical Device (IVD) is regulated as medical device since 1987, and the implementation of IVD registration was fully completed in 2005. The management system of IVD medical device is highly similar with a
Publikováno v:
Expert Review of Medical Devices. 13:533-543
With the aging of the post-war baby boomer generation, the increasing demands for healthcare are driving the growth of medical industry and development of new products in order to meet the immense needs from the aging population. However, medical dev
Publikováno v:
BioMed Research International, Vol 2015 (2015)
BioMed Research International
BioMed Research International
The implementation of an effective quality management system has always been considered a principal method for a manufacturer to maintain and improve its product and service quality. Globally many regulatory authorities incorporate quality management