PHARMACEUTICAL
REGULATORY AFFAIRS
IN LATIN AMERICA

Conference Date: 02 Nov 2009-18 Dec 2009
Conference Ref: A11-6009
Fee: £1590 + VAT
Venue: The Cavendish Hotel, London

A comprehensive review of the evolving regulatory environment, emphasising the challenges and opportunities for the Pharmaceutical Industry in key Latin American countries

You will cover during the 3 days:

• Latin America Demographics and Market Characteristics
• Currently Applicable Legislation for Key LA Countries
• Product Marketing Authorisation Requirements: NCE similar Drugs and Generics
• Stability Requirements
• Site Inspections
• Packaging and Labelling
• Marketing Authorisation Modifications Requirements
• Interactive Workshops: Putting Learning into Practice

Chaired by Arturo Gonzáles-Martinez - PhD Director, Regulatory Affairs GlaxoSmithKline, Mexico

Speakers:

Sofia Nuñez, BSc - Regional Regulatory Affairs Manager - Latin America, Merck& Co., Inc., Mexico
Marcelo Lima, MD - Director, Thema Consultoria Empresarial, Brazil

Click here  to register for this important annual update

This seminar will be of particular interest to all those who need to learn about successful marketing authorisation applications and in-market regulatory compliance including:

Scientists and Technical Personnel in:

• Regulatory Affairs
• Registration Departments
• Medical Directors
• Analytical Research and Development
• Quality Assurance
• New Business Development Departments
• Regulatory Authorities

Click here  to register for this important annual update