|List Name||Medical device quality and regulatory issues (Medical Devices)|
|Purpose:||The purpose of this list is to encourage discussion and problem solving for all those involved in the medical devices or in vitro diagnostics industries who are concerned with or interested in the quality and regulatory aspects of these products.
Topics to be included include ISO 9000, EN 46000, ISO 13485, European directives such as the MDD and IVDMDD, Notified bodies, Canadian regulations and US FDA requirements.
This list is by no means exhaustive and messages are welcome on all regulatory and quality aspects of medical devices.
|List Type:||Unmoderated discussion|
|Subscription:||Requires owner approval|
|Archive:||Readable by anyone|
|Created:||Oct 08, 2001|
|To Join:||Subscribe here, or send an email to firstname.lastname@example.org|
|To Post:||Send mail to 'email@example.com'|
|Stats:||86 subscribers / < 1 messages per week|
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