APPLY NOW (23/8)Medical Device Regulatory Certificate
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APPLY NOW (23/8)Medical Device Regulatory Certificate
課程編號: MDRC11P1
課程名稱: APPLY NOW
(23/8)Medical Device Regulatory Certificate
簡介: ** Course Details **
Global and Regional Regulatory Environment
Asia Medical Device Regulatory Overview
Medical Device Definition and Classification
HK Medical Device Regulatory Detail and Case Study
入學要求: Interested Parties
開課日期: 23 August 2011
上課時間: 23 August 2011 9:30am - 17:30pm
上課地點: 15/F, Bamboos Centre, 52 Hung To Road, Kwun Tong, Kowloon, Hong Kong
費用: $5800
截止報名日期:
查詢: 2575 5903 (Miss Lau)
傳真: 27781810
相關講座:
課程單張:
備註:
>>Click Here to Download Application Form<<
Medical Device industry is a highly regulated industry. We would recommend commercial team and of course regulatory team to get systemic and formal training in order to understand the regulations related to medical device importation, distribution, promotion and registration etc.
With the success of regulatory trainings done in HK and Asia by Jack Wong, we have more than 700 graduates including participants from Government Officials, Industry Colleagues, University Students, Retailers, Lawyers, Consultants etc.
Trainer: ?Mr.?Jack WONG
Currently the Director, Regulatory Affairs in Johnson & Johnson Medical
Over 16 years of Regulatory, Clinical Trial and Pharmacovigilence experience in Asia with good knowledge in the field of Cancer products, Pharmaceuticals, Nutritional products, Medical Devices, Consumer Healthcare and Biological. Managed 400 medical device and 215 pharmaceutical?registration projects with 32 regulatory related staff and consultants in 18 countries of Asia. Direct reports include 12 Regulatory staff range from senior assistant to managerial level.
Externally, playing a leading role among all the Regional Regulatory professionals in AHWP (Asian Harmonization Working Party), and was invited to provide regulatory training to local universities and industry organizations.
Course Details:
Global and Regional Regulatory Environment
Asia Medical Device Regulatory Overview
Medical Device Definition and Classification
HK Medical Device Regulatory Detail and Case Study
Date:?23 Aug 2011 (9:30am – 5:30pm)
Organizer:?ARPA (Asia Regulatory Professional Association)
Venue:?15/F, Bamboos Centre, 52 Hung To Road, Kwun Tong, Kowloon, Hong Kong
Fee:?HK$5800 per person (20% discount to HKAPI* and HKMHDIA** members) [Paypal available]
*HKAPI: The Hong Kong Association of the Pharmaceutical Industry
**HKMHDIA: Hong Kong Medical and Healthcare Device Industries Association
課程名稱: APPLY NOW
(23/8)Medical Device Regulatory Certificate
簡介: ** Course Details **
Global and Regional Regulatory Environment
Asia Medical Device Regulatory Overview
Medical Device Definition and Classification
HK Medical Device Regulatory Detail and Case Study
入學要求: Interested Parties
開課日期: 23 August 2011
上課時間: 23 August 2011 9:30am - 17:30pm
上課地點: 15/F, Bamboos Centre, 52 Hung To Road, Kwun Tong, Kowloon, Hong Kong
費用: $5800
截止報名日期:
查詢: 2575 5903 (Miss Lau)
傳真: 27781810
相關講座:
課程單張:
備註:
>>Click Here to Download Application Form<<
Medical Device industry is a highly regulated industry. We would recommend commercial team and of course regulatory team to get systemic and formal training in order to understand the regulations related to medical device importation, distribution, promotion and registration etc.
With the success of regulatory trainings done in HK and Asia by Jack Wong, we have more than 700 graduates including participants from Government Officials, Industry Colleagues, University Students, Retailers, Lawyers, Consultants etc.
Trainer: ?Mr.?Jack WONG
Currently the Director, Regulatory Affairs in Johnson & Johnson Medical
Over 16 years of Regulatory, Clinical Trial and Pharmacovigilence experience in Asia with good knowledge in the field of Cancer products, Pharmaceuticals, Nutritional products, Medical Devices, Consumer Healthcare and Biological. Managed 400 medical device and 215 pharmaceutical?registration projects with 32 regulatory related staff and consultants in 18 countries of Asia. Direct reports include 12 Regulatory staff range from senior assistant to managerial level.
Externally, playing a leading role among all the Regional Regulatory professionals in AHWP (Asian Harmonization Working Party), and was invited to provide regulatory training to local universities and industry organizations.
Course Details:
Global and Regional Regulatory Environment
Asia Medical Device Regulatory Overview
Medical Device Definition and Classification
HK Medical Device Regulatory Detail and Case Study
Date:?23 Aug 2011 (9:30am – 5:30pm)
Organizer:?ARPA (Asia Regulatory Professional Association)
Venue:?15/F, Bamboos Centre, 52 Hung To Road, Kwun Tong, Kowloon, Hong Kong
Fee:?HK$5800 per person (20% discount to HKAPI* and HKMHDIA** members) [Paypal available]
*HKAPI: The Hong Kong Association of the Pharmaceutical Industry
**HKMHDIA: Hong Kong Medical and Healthcare Device Industries Association
kenkenken- 文章數 : 13
注冊日期 : 2011-08-03
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