3-hr Virtual Seminar: Emerging FDA and EU Trends in IVD Regulatory Compliance (Medical DeviceTraini)
Venue: Online Event
|Event Date/Time: Oct 21, 2011||End Date/Time: Oct 21, 2011|
Significant changes in statutory, regulatory and Agency policies relating to medical devices, generally and in vitro diagnostic products in particular are currently underway.
This interactive virtual seminar will cut through the legislative and regulatory clutter, the jargon being used and array of policy changes for IVD products. Webinar participants will gain a solid understanding of the broad initiatives as well as the key regulatory issues and policies that will shape IVD device registration and compliance for the foreseeable future. Emphasis will be placed on detailed requirements and practical strategic options that regulatory, quality and development professionals will need to avoid costly problems in bringing new IVD products to market in the next three to five years.
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