2025-04-24 2025-04-24 , online online, 1,990 € zzgl. MwSt. Anita Patel https://forum-institut.de/seminar/25092510-marketing-authorisation-in-latin-america/referenten/25/25_09/25092510-course-marketing-authorisation-in-latin-america_patel-anita.jpg Marketing Authorisation in Latin America

An interactive online seminar to explore real regulatory cases and challenges in marketing authorisation and lifecycle management across Mexico, Argentina, Colombia, Peru, Chile and Brazil - led by local experts from Brazil and Peru.

Topics
  • LATAM pharmaceutical landscape: market potential, harmonisation trends and regional dossier formats
  • National procedures and updates in Brazil, Mexico, Argentina, Colombia, Chile and Peru
  • Dossier requirements for NCEs, generics and orphan drugs
  • - Lifecycle management: variations, renewals, labelling and inspection readiness
  • Fast-track initiatives, digitalisation, reliance models and mutual recognition
  • Case-based learning: practical exercises, country-specific challenges and cross-country strategy


Who should attend
This online seminar is designed for professionals working in Regulatory Affairs and related departments who are involved in marketing authorisation and product maintenance for Latin American markets.

The seminar will focus on human medicinal products (chemicals and biologics; herbals will not be addressed).

Basic understanding in regulatory affairs is required.
Aims and objectives
What are the key success factors in introducing your products in the LATAM region? What do you need to consider when applying for marketing authorisation in countries such as Brazil, Mexico, Argentina or Peru? This online seminar will equip you with the knowledge to answer these questions.

Two seasoned LATAM experts will guide you through the region’s complex regulatory landscape, offering first-hand insights into dossier requirements, authorisation procedures and maintenance duties. Through interactive case studies and group discussions, you will explore market-specific challenges and receive practical tools for your day-to-day regulatory work. You’ll also benefit from expert tips on fast-track options, reliance strategies, and dossier format differences.

The combination of theoretical input and practical application ensures a deep understanding of the regulatory affairs business in Latin America - empowering you to develop more effective market access strategies.
Your benefit

  • Meet experts with local know-how and firsthand experience
Gain deep insights into Brazilian, Mexican, Colombian and Argentinian markets
Understand key dossier requirements and regulatory procedures
Learn how to navigate fast-track options and reliance strategies
Discuss real-world cases and bring your own challenges
Strengthen your LATAM regulatory strategy with practical tools

Course Marketing Authorisation in Latin America

Marketing Authorisation in Latin America

Focused insights on regulatory strategies in Brazil, Mexico, Argentina, Colombia, Chile and Peru

Benefits
  • Local experts for firsthand information
  • Fast-track options and reliance strategies
  • Key dossier requirements and regulatory procedures
  • Officially certificated ISO 9001 and ISO 21001

Webcode 25092510

Jetzt buchen

JETZT Buchen

Referenten


Alles auf einen Blick

Termin

24-25/09/2025

24-25/09/2025

Zeitraum

from 10:00 - 18:00 on both days, You may dial in 30 min. before the session

from 10:00 - 18:00 on both days, You may dial in 30 min. before the session
Veranstaltungsort

online

online

Downloads
Gebühr
Your contact

Verena Planitz
Conference Manager

+49 6221 500-655
v.planitz@forum-institut.de

Details

An interactive online seminar to explore real regulatory cases and challenges in marketing authorisation and lifecycle management across Mexico, Argentina, Colombia, Peru, Chile and Brazil - led by local experts from Brazil and Peru.

Topics

  • LATAM pharmaceutical landscape: market potential, harmonisation trends and regional dossier formats
  • National procedures and updates in Brazil, Mexico, Argentina, Colombia, Chile and Peru
  • Dossier requirements for NCEs, generics and orphan drugs
  • - Lifecycle management: variations, renewals, labelling and inspection readiness
  • Fast-track initiatives, digitalisation, reliance models and mutual recognition
  • Case-based learning: practical exercises, country-specific challenges and cross-country strategy


Who should attend
This online seminar is designed for professionals working in Regulatory Affairs and related departments who are involved in marketing authorisation and product maintenance for Latin American markets.

The seminar will focus on human medicinal products (chemicals and biologics; herbals will not be addressed).

Basic understanding in regulatory affairs is required.

Aims and objectives

What are the key success factors in introducing your products in the LATAM region? What do you need to consider when applying for marketing authorisation in countries such as Brazil, Mexico, Argentina or Peru? This online seminar will equip you with the knowledge to answer these questions.

Two seasoned LATAM experts will guide you through the region’s complex regulatory landscape, offering first-hand insights into dossier requirements, authorisation procedures and maintenance duties. Through interactive case studies and group discussions, you will explore market-specific challenges and receive practical tools for your day-to-day regulatory work. You’ll also benefit from expert tips on fast-track options, reliance strategies, and dossier format differences.

The combination of theoretical input and practical application ensures a deep understanding of the regulatory affairs business in Latin America - empowering you to develop more effective market access strategies.

Your benefit

  • Meet experts with local know-how and firsthand experience
Gain deep insights into Brazilian, Mexican, Colombian and Argentinian markets
Understand key dossier requirements and regulatory procedures
Learn how to navigate fast-track options and reliance strategies
Discuss real-world cases and bring your own challenges
Strengthen your LATAM regulatory strategy with practical tools

Detailed programme

from 10:00 - 18:00 on both days, You may dial in 30 min. before the session

Anita Patel

Welcome and introductions
  • Participant ice-breaker: Experience in LatAm registrations
  • Objectives and seminar overview

Anita Patel

Latin American pharmaceutical landscape: Market insights and regulatory environment
  • Market potential: Mercosur, Pacific Alliance
  • Harmonisation trends: AMLAC, ICH alignment, reliance pathways
  • Overview of common dossier formats: CTD, eCTD, local adaptations
  • Insights on smaller markets: Central America, Ecuador, Uruguay, etc.
  • Fastest approval process?

Anita Patel

Brazil: Marketing authorisation and lifecycle management
  • ANVISA procedures and updates
  • Dossier requirements: NCEs, generics, biologics, biosimilars
  • Orphan drug procedures and reliance opportunities
  • Maintenance: Variations, renewals, labelling
  • Preparing for ANVISA inspections

All

Practical exercise: Case study for Brazil
  • Interactive scenario discussion

Bertha Cabrera Lavado

Mexico: Marketing authorisation and lifecycle management
  • COFEPRIS procedures and recent reforms
  • Dossier requirements: NCEs, generics, biologics, biosimilars
  • Orphan drug procedures and reliance opportunities
  • Maintenance: Variations, renewals, labelling
  • Fast-track initiatives and digitalisation

Practical exercise: Case study for Mexico
  • Interactive scenario discussion

Bertha Cabrera Lavado

Argentina: Marketing authorisation and lifecycle management
  • ANMAT procedures and dossier specifics
  • Dossier requirements: NCEs, generics, biologics, orphan drugs
  • Fast-track routes and regulatory simplifications
  • Maintenance: Variations, renewals, labelling

Practical exercise: Case study for Argentina
Interactive scenario discussion

Anita Patel

Day 2
  • Key Takeaways & Open Questions from Day 1

Anita Patel

Colombia: Marketing authorisation and lifecycle management
  • INVIMA procedures and dossier specifics
  • Dossier requirements: NCEs, generics, biologics, orphan drugs
  • Maintenance: Variations, renewals, labelling

Practical exercise: Case study for Colombia
  • Interactive scenario discussion

Bertha Cabrera Lavado

Chile: Marketing authorisation and lifecycle management
  • ISP procedures and dossier specifics
  • Dossier requirements: NCEs, generics, biologics, orphan drugs
  • Maintenance: Variations, renewals, labelling

Practical exercise: Case study for Chile
  • Interactive scenario discussion

Bertha Cabrera Lavado

Peru: Marketing authorisation and lifecycle management
  • DIGEMID procedures and dossier specifics
  • Dossier requirements: NCEs, generics, biologics, orphan drugs
  • Maintenance: Variations, renewals, labelling

Practical exercise: Case study for Peru
  • Interactive scenario discussion

Bertha Cabrera Lavado, Anita Patel

Cross-country comparison and strategy session
  • Comparative recap: Approval timelines, dossier formats, renewal periods
  • Multi-country filing strategies and mutual recognition

Bertha Cabrera Lavado, Anita Patel

Take Home Messages

Bertha Cabrera Lavado, Anita Patel

Expert panel: Live Q&A session

Your options:

In-house training on "Marketing Authorisation in Latin America"

Are you interested in an in-house training course on topic "Marketing Authorisation in Latin America"? Please contact us to find out more.

More information

Access to and procedure for online events

Once you have registered for an event, we will send you the access information for your customer portal. Click here to log in to the customer portal using your email address and password. Please ensure you can access the customer portal before the day of the event.

All important or additional information and personal documents are available in your personalised customer portal. This is also where you start your online courses. If you do not have access to the customer portal yet, you can easily register here.

On the day of the event, you kick off your online training in the customer portal by clicking ‘Participate’ directly in the respective event. You will then be redirected to the Learning Space.

Learn more about our online events here.

Free pre-meeting and technology check

You can attend one of our pre-meetings and explore our Learning Space free of charge. Registration is not required. You can find available dates for a pre-meeting in your customer portal. Click the green ‘Participate’ button in the pre-meeting in the customer portal and you will be redirected to the Learning Space.

The pre-meeting gives you the opportunity to explore our Learning Space and to familiarise yourself with the technology to start off your online training on the right foot. This is a non-binding offer for all our customers and not a prerequisite for participation. If a pre-meeting date does not suit you but you would still like a technology check, please contact us.

Technical requirements

You need a reliable Internet connection to take part in our online events. To have the best possible learning experience, we recommend that you use the latest version of the Microsoft Edge or Google Chrome browsers. You will need a headset, loudspeaker or telephone to play the audio. Further information is available here. Please check beforehand that your microphone or headset and camera are working properly. Do not access our services from a VPN since there are issues with the audio over such connections.

We have integrated Zoom video conferencing software into our Learning Space for our online training courses. If you are not authorised to use Zoom, please get in touch with us so we can make alternative arrangements for you to take part in our online training.

Looking to train several employees on this topic?

We offer customised in-house training! Take advantage of our proven seminar concepts and ensure your team reaches a unified level of knowledge quickly and efficiently. We’d be happy to provide you with a non-binding offer.

Please contact Verena Planitz (v.planitz@forum-institut.de) for more information!

This distinguishes our events

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)

Recommendations

CMC Management in Regulatory Affairs

This online training will give you in-depth knowledge on the CMC requirements for marketing authorisation. Take the chan...

22. - 23.05.2025 in
Details

Medical Writing in Pharmacovigilance

Enhance your skills in writing key pharmacovigilance safety documents. In this two-day online seminar, you will gain a c...

19. - 21.05.2025 in
Details

Biopharmaceuticals

The compact course with a content focus on the development, production and analytics of biotech drugs. Secure your place...

03. - 05.06.2025 in
Details

An Introduction for Pharmacovigilance Managers

Are you new to pharmacovigilance and looking to kick-start your career? Then this online course is just for you. Gain a ...

28. - 29.04.2025 in
Details

Regulatory Lifecycle Management

This course familiarises you with regulatory post-approval duties and provides first-hand information on variation submi...

04.06.2025 in
Details

Go forward

Pharma FORUM Webcast International

International experts will inform you of the latest trends in global marketing authorisation and drug safety every two m...

Details
Pharma FORUM Webcast International
Newsletter

FORUM Institut provides the latest news on various relevant topics in its newsletter. We bring you up to date with the l...

Details
Newsletter
We guarantee the highest quality

We are now officially certified to ISO 9001 and ISO 21001 standard.

Details
We guarantee the highest quality

Testimonials

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