Conference & Events
Event Details
Live webinar on Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By compliance2go
understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products.
Date: 04 June 2012 01:00 - 02:30
Event Subject(s):
General
Venue
Online
10777 Westheimer Suite 1100
Houston, Texas
77042
United States of America
Find this location using Google Map
Useful link:
https://compliance2go.com/index.php?option=com_training...
Organiser Information
Organiser(s): Compliance2go
Contact for Event Information
Name : Miss Trisha Paul
Address:
10777 Westheimer Suite 1100
Houston, Texas
77042
United States of America
Tel:
18777824696
Fax:
281-971-0286
Email:
subscribe@compliance2go.com
Contact Useful link:
https://compliance2go.com/index.php?option=com_training...
Additional Information
Speaker Information:
Robert J. Russell, is President and CEO of RJR Consulting, Inc, a leading Global Regulatory Consulting firm focusing on assisting the Life Science Industry. Prior to founding the firm in 2000, Mr. Russell had over 27 years of experience in CMC, Global Business Development and Regulatory Compliance for pharmaceuticals, biologics, medical devices and combination products. The company has an office in Brussels, Belgium where they interact with the European Commission and the Competent Authorities across the EU. Country establishment, marketing authorizations, variations and license renewals are core competencies of the course director. Mr. Russell has received a B.S. and M.S.in Chemistry.
Useful link:
https://compliance2go.com/index.php?option=com_training...
