•The Regulatory Affairs Journal Devices - medical device & in v...
Regulatory Affairs Journal Devices back issues information: With the increasing importance and development of Medical Devices and in vitro Diagnostics, RAJ Devices was established as a sister publication to RAJ, in 1993.
•Canadian Medical Device Regulation Consultants - CMDR
Medical device quality & regulatory consultants for Canadian medical device regulations, device licensing, FDA compliance, 510k, CE Marking, ISO 14971 & EU Authorized Representative for Europe. Offices in Toronto and Vancouver.
•Health Industries: Medical Device Industry
Through domestic and international industry analysis and policy development, the International Trade Administration's health team helps health industries to identify, access, and better compete in global markets.
•Medical Device and Equipment Resource Center
Medical equipment buyers, sellers and dealers. Resource center contains governmental regulations, references, organizations. Information on medical equipment in China
•Regulation of medical device/medicine 'boundary' products
On 21 April 2004 the TGA gazetted the Therapeutic Goods (Articles that are not Medical Devices) Order No. 1 of 2004 under Section 41BD(3) of the Therapeutic Goods Act 1989. Implementing the following changes to the way the TGA reg...
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