This webinar will discuss the regulatory structure and requirements for compliance with Chinese SFDA regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products.
This 3-hr virtual seminar will discuss the requirements and compliance in medical device adverse event reporting and medical device surveillance/vigilance system in the US, Europe and Canada.
This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America.
Post market surveillance is changing, not only in the US, but also in the EU and Canada.
Download events tagged medical devices in XML or iCalendar format.
The Boxes and Arrows event calendar is a place to find events of interest to designers. These can be specific design events, such as an AIGA event, SXSW or the IA Summit, part design/part other, such as Webvisions or it can be tangentially related, such as a business event or one on CSS.
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