Export Certificate for Medical Devices - Out Your Competition!

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 PresentationBackgroundUse of export certificatesTypes of Certificates (including Export permit)How to choose a certificate typeHow to request Processing
Who Will Benefit:Clinical Trial Physician / DoctorManager to Senior Director ofRegulatory AffairsQuality AssuranceClinical ResearchData ManagementData MonitoringInstitutional Review Board
Speaker Profile:Angela Bazigos is the CEO of Touchstone Technologies Inc. She has degrees in Microbiology and Computing and 40 years of experience in the Life Sciences, Healthcare & Public Health Services. Experience combines Quality Assurance, Regulatory Compliance, Business Administration, Information Technology, Project Management, Clinical Lab Science, Microbiology, Food Safety & Turnarounds. Past employers / clients include Royal Berkshire Hospital, Roche, Novartis, Genentech, PriceWaterhouseCoopers & Stanford Hospital.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14@gmail.com