Netzealous LLC DBA - Compliance4All, Online
2019-03-20
Overview: The rules that companies must follow when exporting medical devices depend on whether or not their devices have been approved or cleared by the Food and Drug Administration.
Why should you Attend: In submitting export certificates, any mistake, no matter how minor, can delay product approvals, launches, or cause widespread public relations disasters. Therefore, understanding and correct execution of the export certificate processes has become a competitive advantage for global manufacturers of medical devices.
Areas Covered in the Session: Purpose of Presentation Background Use of export certificates Types of Certificates (including Export permit) How to choose a certificate type How to request Processing
Who Will Benefit: Clinical Trial Physician / Doctor Manager to Senior Director of Regulatory Affairs Quality Assurance Clinical Research Data Management Data Monitoring Institutional Review Board
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: compliance4all14@gmail.com
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