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Searching Content indexed under Media, Telecoms, IT, Entertainment by Eileen McMahon ordered by Published Date Descending.
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Look Before You Leap: Pre-Canadian Launch Regulatory Considerations For U.S. Companies
Deciding whether or not to launch a food, drug, medical device, dietary supplement or cosmetic product in Canada involves a number of considerations.
Canada
20 May 2014
2
Considerations For Medical Device Software Companies Entering The Canadian Market
Canada has one of the world’s largest medical device markets, estimated at C$6 billion in 2010, with sales of almost C$3 billion taking place in Ontario. he medical device industry in Canada, not taking into account medical imaging and assistive devices, employs over 35,000 people in about 1,500 companies, the bulk of which are small or medium-sized companies.
Canada
27 Jul 2011
3
Deadline for Compliance of Medical Device Software in Canada: February 1, 2011
The Medical Devices Bureau of Health Canada (the Bureau) expects that all Class I Medical Device software marketed in Canada will be compliant with the Medical Devices Regulations (the Regulations) by February 1, 2011, and all Class II Medical Device software will be compliant by September 1, 2011.
Canada
18 Jan 2011
4
Canadian and U.S. Regulation of Functional Food Claims
In today’s health-conscious marketplace, functional food labelling has grown into a multibillion dollar industry.
Canada
13 Oct 2010
5
Classify Patient Management Software in Canada
Health Canada has Clarified the approach taken by its Medical Devices Bureau to Classify Patient Management Software as Either A Class I Or A Class II Medical Device
Canada
21 Jun 2010
6
Classifying Medical Device Software In Canada
Health Canada has indicated that it plans to release an updated notice on classifying patient management software in the coming weeks, modifying the notice it released on August 31, 2009.
Canada
18 Mar 2010
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