Online seminar with a focus on: Brazil, Mexico, Argentina, Colombia, Peru
Webcode 24092510
Esther Gil López
PAREXEL Consulting, Madrid, ESPANIA
Regulatory affairs Director South Europe and Latin America Esther Gil López has 22 years' experience working in Regulatory Affairs, from early phase to late phase clinical trials across all regions, as well as in the provision of scientific and technical support on matters related to product development and marketing approval of drug products. Currently, she manages large international teams of regulatory professionals in Southern Europe and Latin America.
Anita Patel
Parexel International, São Paulo, BRAZIL
Pharmacist and Biochemist, Regulatory Affairs Director Anita has tenyears' experience in regulatory affairs consulting and leads the Latin American regulatory and publishing team in Argentina, Brazil, Chile, Colombia, Mexico and Peru. Together with other experts in Latin America, Anita oversees and acts as project lead for regulatory support provided to pharmaceutical companies for the submission of marketing authorisation applications, registration maintenance, marketing authorisation transfers, regulatory strategy for submissions, GAP analyses and regulatory intelligence reports for Latin American countries. Prior to consulting, Anita gained 12 years' experience in regulatory affairs in the Brazilian pharmaceutical industry.
26-27/09/2024
26-27/09/2024
from 10:00 - 18:00 on both days, You may dial in 30 min. before the session
online
online
Event - 1,890 € plus tax
The fee includes a comprehensive online documentation and a certificate
Event - 1,890 € plus tax
The fee includes a comprehensive online documentation and a certificate
Verena Planitz
Conference Manager
+49 6221 500-655
v.planitz@forum-institut.de
An online seminar to discuss real cases/challenges for marketing authorisation in Mexico, Argentina, Colombia, Peru, Chile and Brazil with local experts from Brazil and Spain.
What are the key success factors in introducing your products in the LATAM region? What do you have to keep in mind when applying for a marketing authorisation in these countries?
This online seminar will enable you to answer these questions and will provide deep insights into the regulatory environments of the various markets.
Two LATAM experts will share valuable information regarding:
10:00 Introductions and agenda
10:30
Esther Gil López
11:30 Coffee break
11:40
Esther Gil López
12:40 Lunch
13:40
Esther Gil López
14:10
All
14:30 Coffee break
15:00
Anita Patel
16:30 Short break
16:40
Anita Patel
17:10
All
17:30
Anita Patel
18:00 End of day 1
10:00
Esther Gil López
11:00
All
11:20 Coffee break
11:30
Esther Gil López
12:20
All
12:30 Lunch
13:30
Anita Patel
14:30 Coffee break
14:40
All
15:00
Anita Patel
16:00
All
16:20 Short break
16:30
Anita Patel
17:30
All
18:00 End of seminar
Log in to the customer portal at https://members.forum-institut.de/login with your username (email address) and password. Please ensure that you can access the customer portal prior to the event. On the day of the event, you will kick off your online training in the customer portal by clicking 'Participate' in the respective event.
Overall impression: 100 % of the participants' feedback was very good or good (September 2022)
Course content: 100 % of the participants' feedback was very good or good (September 2022)
Would you like to successfully approve and market your medical devices in China as well? Then attend our webcasts and le...
Enhance your skills in writing key pharmacovigilance safety documents. In this two-day online seminar, gain not just a b...
The compact course with a content focus on the development, production and analytics of biotech drugs. Secure your place...
LAST CALL! - CANCELLATION DEADLINE: 29.04.2024 - Variation regulation, classification guideline, eSubmission, variation ...
Regulatory expectations regarding risk management for pharmaceuticals in (emerging) markets often contend with the strin...
International experts will inform you of the latest trends in global marketing authorisation and drug safety every two m...
Details
With this qualification course, you can continue your education in a structured manner in all global regulatory affairs ...
Details
We are now officially certified to ISO 9001 and ISO 21001 standard.
Details
This seminar deals with regulatory aspects in Latin American countries. The seminar is conducted by very experienced speakers from Spain and Brazil. There are practical activities that enable you to deepen the knowledge you have acquired. The seminar left a very positive impression in terms of the knowledge imparted and the technical competence of the speakers.
Both speakers were great!
I wanted to get a comprehensive overview of the regulatory issues in Latin American countries. The seminar exceeded my expectations
Brazil requirements very helpful
Andrea and Esther did a very good Job; I expected an overview about the regulations and specific issues, and I get one.
Specific questions relating to Brazil - expectation met
