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Handbook of Medical Device Regulatory Affairs in Asia
ISBN/GTIN

Handbook of Medical Device Regulatory Affairs in Asia

E-bookPDFDRM AdobeE-book
EUR129,99

Product description

Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put in place new regulatory systems or refined the existing ones. A registered product requires a lot of technical documentation to prove its efficacy, safety, and quality. A smooth and successful registration process dem
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Details

Additional ISBN/GTIN9789814411226
Product TypeE-book
BindingE-book
FormatPDF
Format noteDRM Adobe
Publishing date27/03/2013
LanguageEnglish
File size13741 Kbytes
Article no.6748369
CatalogsVC
Data source no.792096
Product groupBU691
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Author

Jack Wong is the founder of the Asia Regulatory Professional Association (ARPA) and the Asia GRP (Good Regulatory Practice) Research Centre. He has more than 18 years of experience in regulatory affairs, clinical trials, and pharmacovigilence in Asia and possesses good knowledge of medical devices, pharmaceuticals, and nutritional, consumer healthcare, and biological products. Prof. Wong developed the first Asia Regulatory Affairs Certificate course in 2007.