Emergo Group Medical Device Regulatory 2.2
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ABOUT Emergo Group Medical Device Regulatory
A valuable reference tool for medical device Regulatory Affairs (RA) and Quality Assurance (QA) professionals. Quick access to global medical device regulations, daily medical device regulatory updates, contact information for 60+ Ministries of Health and Certification Bodies. Emergo's mobile app contains valuable reference information for regulatory and quality assurance professionals. Here's what you will get: Latest regulatory updates from the Emergo blog Quick access to device regulations for 20+ countries Downloadable flow charts, white papers plus videos Plus, the app contains fully interactive copies of the following regulations, allowing you to quickly jump to relevant sections: US FDA 21 CFR Part 820 (Also includes parts 801, 803, 806, 807, 809, 812, 821, 822, 860) EU MDD 93/42/EEC (Complete with all sections linked for easy access, plus 2007/47/EC) EU IVD Directive (98/79/EC) EU DIRECTIVE 2007/47/EC This app includes regulatory information covering 90% of the global medical device market including: Australia Brazil Canada China Europe Hong Kong India Japan Malaysia Mexico Russia South Korea United States