Jun 2, 2016
North America
The FDA is in the process of implementing the Unique Device Identification (UDI) System in a series of phases. Currently, all Class III and implantable, life-supporting and life-sustaining medical devices require UDIs. The next phase of the system will be implemented...
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May 24, 2016
North America
Mobile health app The growing significance of mobile health apps result in a need to ensure its proper regulation. Practitioners, patients, researchers and medical industries are all affected by mHealth apps. The digital health field is regulated by the FDA under four...
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May 11, 2016
Consultant Post
China has become the second largest medical device market in the world. Sustained economy, population growth and a burgeoning aging population makes China a lucrative market for foreign medical device and pharmaceutical manufacturers. Nevertheless, China is considered...
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Jan 27, 2016
Europe
The Eurasian Economic Commission (EEC) is the permanent regulatory body of the Eurasian Economic Union (EEU). The EEU was established as part of a treaty in 2014 and signed by Belarus, Kazakhstan, Russia, Armenia and Kyrgyzstan. The EEU, much like the EU, aims to...
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Jan 13, 2016
Asia
China has a Revised Drug GSP, ensure your
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