Netzealous LLC DBA - Compliance4All, Online
2018-02-14
Overview: This webinar will address the four key steps to compliance by device
manufacturers. Also covered will be the Final Rule's provisions to
address existing FG inventory, not properly labeled.
Why should you Attend: It will also review the implementation schedule which is required of
medical device companies selling products in the U.S. This is a major
change for medical device manufacturers, with far-reaching effects in
regulatory compliance, as envisioned by the FDA.
Areas Covered in the Session: Learn the basic requirements of UDI Labeling and its Database UDI / GUDID Implementation Schedules Required steps for UDI / GUDID compliance by the Medical Device
Company Future Requirements
Who Will Benefit: Process Validations CGMP Responsibilities CROs and Clinicals Personnel Medical Personnel Other Healthcare Professionals Staff and Office Personnel
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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