U.S. Device Makers Seek Exemptions From Korean Device-Testing Rules
This article was originally published in PharmAsia News
Executive Summary
U.S. device manufacturers are pleased with recent changes in good manufacturing practice regulations (GMPs) made by the Korean Food and Drug Administration, but are seeking exemptions from new product testing requirements, according to AdvaMed
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A regular roundup of commercial stories appearing in Scrip’s sister publication PharmAsia News, whose multilingual team of regional experts provides authoritative business intelligence focused on the Asian marketplace. Full stories can be accessed by clicking on the story title (subscription required).
PharmAsia News Business Bulletin
A regular roundup of commercial stories appearing in Scrip’s sister publication PharmAsia News, whose multilingual team of regional experts provides authoritative business intelligence focused on the Asian marketplace. Full stories can be accessed by clicking on the story title (subscription required).
PharmAsia News Business Bulletin
A regular roundup of commercial stories appearing in Scrip’s sister publication PharmAsia News, whose multilingual team of regional experts provides authoritative business intelligence focused on the Asian marketplace. Full stories can be accessed by clicking on the story title (subscription required.)