Export Certificate for Medical Devices - Out Your Competition!

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Category Regulatory Affairs, Quality Assurance, Clinical Research, Data Monitoring

Deadline: March 19, 2019 | Date: March 20, 2019

Venue/Country: Online, U.S.A

Updated: 2019-01-21 15:11:15 (GMT+9)

Call For Papers - CFP

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

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: +1-800-447-9407

Email: compliance4all14gmail.com