Presented by
Management Forum
This programme offers a detailed examination of the regulatory landscape, emphasizing both challenges and opportunities for the pharmaceutical industry across key Latin American markets, including Argentina, Brazil, Chile, Colombia, Mexico, and Peru.
22 October 2024
+ 25 February 2025 »
from £549
Explore and gain insights into the regulatory framework of the main authorities in key Latin America countries (Brazil, Mexico, Colombia, Chile, Argentina and Peru).
Pharmaceutical products undergo evaluation based on the regulatory requirements outlined by each country for their sanitary registration. The Latin American region faces significant regulatory challenges due to the absence of a unified and standardized procedure among authorities. Each regulatory body has its own set of regulations, making it daunting to navigate through the diverse legal frameworks. In this course, participants will gain insights into the specific regulations of each country, delve into various approaches to obtaining marketing authorization, and analyse commonalities and differences among the most advanced regulatory authorities in Latin America.
Throughout the training, participants will engage in in-depth case studies to explore options and strategies for fulfilling crucial regulatory activities. This interactive learning experience will provide opportunities to discuss and exchange experiences with our expert trainer and fellow delegates.
This course is part of our Regulatory Affairs Training course collection, which features updates on the latest regulations to registration procedures and strategies.
Key topics to be addressed:
This seminar will be of particular interest to all those who need to learn about successful marketing authorisation applications and in-market regulatory compliance in this region. You will find this seminar useful both as an introductory or refresher course.
Pharmaceutical Chemist graduated from Universidad Central de Venezuela, with more than 15 years of experience in the Pharmaceutical Industry and solid knowledge in the life cycle of medicines. Proficient in the different categories and types of products (new, innovative, generic and specific), medical devices, cosmetics including research, development, authorization and commercialization. I have a postgraduate degree in Drug Health Surveillance, and I play a strategic role in the area of regulatory affairs, leading teams and building links with the health authority in national and international companies in different countries (both Latin American and European region).
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
Please contact us for pricing if you are interested in booking 5 or more delegates
22 October 2024
Live online
09:00-17:30 UK (London) (UTC+01)
10:00-18:30 Paris (UTC+02)
04:00-12:30 New York (UTC-04)
Course code 15178
Until 17 Sep
Not ready to book yet?
for 7 days, no obligation
25 February 2025
Live online
09:00-17:30 UK (London) (UTC+00)
10:00-18:30 Paris (UTC+01)
04:00-12:30 New York (UTC-05)
Course code 15179
Until 21 Jan
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
Colombia
Greece
Ireland
Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to: