Got News to Share? Send 2 FREE Releases ↓
All News Topics | Events By Topic | By Country | By State | By Date

FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes

Submit News
Date: 23-Aug-13 to 23-Aug-13
Location: OnlineEvent / California / United States
Category: Education Healthcare & Pharmaceuticals Conferences & Trade Fairs

This training will provide a solid understanding of FDA Requirements for Device Labeling. Attendees will gain comprehensive knowledge on creation, approval and control of labels and labeling.

Visitors

This webinar is designed for those who perform, supervise, manage, audit, or oversee the creation, approval, control of labels and labeling:
Regulatory Affairs management
Document Control (label generation) professionals
Design Control professionals
Quality Assurance professionals
Sales/marketing management

Exhibitors

Instructor Profile:
Jeff Kasoff, RAC, is the Director of Regulatory Affairs at Life-Tech, Inc., a leading manufacturer of consumables and instrumentation in the urodynamic and pain management fields. Jeff is responsible for oversight of corporate compliance with domestic and international regulations, preparation of submissions, and is primary liaison with regulatory agencies and notified bodies. Jeff began his regulatory career as the first full-time employee of Optex Biomedical, a device start-up, where he initiated their regulatory policies and procedures and prepared their submissions. Jeff received his Regulatory Affairs Certification in 1996.

Go to event website