Medical device labeling in the European Union (EU) continues to challenge manufacturers who must create compliant Instructions For Use in all required languages. The latest proposed revisions (to Directive 93/42/EEC and Directive 90/385/EEC) introduce amendments pivotal for e-labeling other devices. The Medical Device E-labeling webinar balances adhering to the e-labeling requirements with creating a winning strategy. Attendees will be exposed to E-labeling compliance requirements within the EU identifying:
- The benefits of E-labeling
- The challenges of E-labeling
- The first steps in developing an e-labeling initiative
Who Should Attend:
Directors, managers and other professionals tasked with developing, planning and executing EU labeling requirements.
Date: March 28th, 2012
Time: 10:00 a.m. CST
To receive more information or register for this webinar, please submit request here, or send a request to webinar@kjinternational.com.