MEDICAL DEVICE
REGULATORY AFFAIRS
IN LATIN AMERICA

Conference Date: 23 Jun 2009-28 Jul 2009
Conference Ref: N6-8209
Fee: £1150 + VAT
Venue: Harrington Hall Hotel, London

This seminar will provide a comprehensive overview of the requirements for successful product approval for medical devices in Latin America.  An ever increasing market, this is an excellent opportunity to learn the processes involved from an experienced consultant in this region.  The programme will cover the regulatory requirements but will also share the interpretation of the regulation, guidance and legislation in these countries that only someone with hands-on experience in the region can provide. It is anticipated that this seminar will be useful both as an introductory course and as a refresher to personnel who need to have up to date and global knowledge of the requirements in this geographical area.

An addition to the programme this year will include a session on effective cross-cultural communication.