Export Certificates for Medical Devices

Website http://bit.ly/1zHCEQ4 | Edit Freely

Category FDA GXP Compliance - Medical Devices;

Deadline: December 12, 2014 | Date: December 12, 2014

Venue/Country: Palo Alto, U.S.A

Updated: 2014-12-09 14:16:10 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

In today’s global environment, sustaining competitive advantage within the medical device industry involves a global product strategy that recognizes the issues involved in managing regulations across different countries. To this end, certain countries require an export certificate that the manufacturer and its devices are indeed in compliance with FDA regulations.

Who Will Benefit:

Clinical Trial Physician/Doctor

Manager to Senior Director of:

Regulatory Affairs

Quality Assurance

Clinical Research

Data Management

Instructor Profile:

Larry Spears is currently an independent consultant and president of L.Spears Consulting, LLC, where he provides regulatory and compliance advice to medical device and pharmaceutical firms in meeting FDA requirements. He also served for over two years as a director in Deloitte & Touche LLP’s Health Sciences practice.

Use coupon code 232082 and get 10% off on registration.