Global Medical Device Regulations - Seminar By ComplianceOnline (Medical Devices)
|Event Date/Time: Sep 13, 2012||End Date/Time: Sep 14, 2012|
This workshop is intended to provide guidance on medical device classification and registration requirements in these countries.
During this workshop (1st day), medical device regulations of twelve countries will be discussed.
On the second day, we will discuss ISO 13485, ISO 14155, ISO 14971, GHTF documents, and MEDDEV guidance documents, etc. for quality and adverse event reporting including group discussions facilitating interpretation, understanding, and implementation of medical device regulations.
Understanding global medical device regulations and requirement and adequate implementation of applicable medical device regulations can significantly expedite the regulatory processes, bringing innovative medical products to the global market faster and saving enormous amount of your unnecessary time, efforts and investment.
At this workshop, you will get familiar with medical device regulations of twelve (12) countries concerning medical devices, active implantable medical devices and in vitro diagnostic medical devices for adequate implementation and successful registration.