2024-07-22 2024-07-22 , online online, 1,190 € zzgl. MwSt. Estefanny K. Da Silva N. https://forum-institut.de/seminar/24122450-cmc-requirements-in-latin-america/referenten/24/24_12/24122450-online-training-course-pharma-cmc-requirements-in-latin-america_da-silva-n-estefanny-k.jpg CMC requirements in Latin America

CMC requirements in Latin America with focus Mexico, Brazil, Colombia, Argentina, Chile, and Peru. The seminar (2 half days) is comfortable to integrate into your daily work routine.

Topics
  • Adaptation from EU and differences within LatAm
  • CMC requirements in Brazil, Mexico, Colombia, Argentina, Chile, Peru: Documentation, country specific requirements, post-approval activities, future trends in the regions


Who should attend
This seminar will be of benefit to all those working in the pharmaceutical industry, particularly CMC and regulatory affairs managers, who are dealing with dossier compilation (quality data/module 3) for regions in Latin America.

The seminar will focus on small molecules.
Aims and objectives
During this seminar you will learn about the specific CMC requirements for the different countries in Latin America with a focus on Brazil, Mexico, Colombia, Argentina, Chile and Peru.

Three (local) experts will share valuable information regarding
  • pharmaceutical documentation;
  • country specific requirements;
  • post-approval activities and
  • future trends.

After the training course you will have gained a better understanding of the additional and differing CMC related requirements and procedures in the different regions.
Your benefit

  • Meet three (local) experts that will share in-depth knowledge with you!
  • Obtain practical CMC know-how for emerging markets!
  • Integrate the two half days onveniently into your daily work routine!
  • Make profit from the practical activity after each talk ("easy learning through application")!

Online training course pharma - CMC requirements in Latin America

CMC requirements
in Latin America

- Online training -

Benefits
  • Experts with local know-how
  • Practical activity after each talk
  • Inform us about your most relevant countries/regions
  • Officially certified according to ISO 9001 and ISO 21001

Webcode 24122450

Jetzt buchen

JETZT Buchen

Referenten


Alles auf einen Blick

Termin

10-11/12/2024

10-11/12/2024

Zeitraum

Day I: 01:00 pm - 5:15 pm - seminar
Day II: 01:00 pm - 5:00 pm - seminar
You may dial in 30 minutes before the training starts

Day I: 01:00 pm - 5:15 pm - seminar
Day II: 01:00 pm - 5:00 pm - seminar
You may dial in 30 minutes before the training starts
Veranstaltungsort

online

online

Gebühr
Your contact

Dr. Birgit Wessels
Conference Manager

+49 6221 500-652
b.wessels@forum-institut.de

Details

CMC requirements in Latin America with focus Mexico, Brazil, Colombia, Argentina, Chile, and Peru. The seminar (2 half days) is comfortable to integrate into your daily work routine.

Topics

  • Adaptation from EU and differences within LatAm
  • CMC requirements in Brazil, Mexico, Colombia, Argentina, Chile, Peru: Documentation, country specific requirements, post-approval activities, future trends in the regions


Who should attend
This seminar will be of benefit to all those working in the pharmaceutical industry, particularly CMC and regulatory affairs managers, who are dealing with dossier compilation (quality data/module 3) for regions in Latin America.

The seminar will focus on small molecules.

Aims and objectives

During this seminar you will learn about the specific CMC requirements for the different countries in Latin America with a focus on Brazil, Mexico, Colombia, Argentina, Chile and Peru.

Three (local) experts will share valuable information regarding

  • pharmaceutical documentation;
  • country specific requirements;
  • post-approval activities and
  • future trends.

After the training course you will have gained a better understanding of the additional and differing CMC related requirements and procedures in the different regions.

Your benefit

  • Meet three (local) experts that will share in-depth knowledge with you!
  • Obtain practical CMC know-how for emerging markets!
  • Integrate the two half days onveniently into your daily work routine!
  • Make profit from the practical activity after each talk ("easy learning through application")!

Detailed programme

Day I: 01:00 pm - 5:15 pm - seminar
Day II: 01:00 pm - 5:00 pm - seminar
You may dial in 30 minutes before the training starts

Welcome, introduction round, expectations


Estefanny Da Silva

LatAm Overview
  • Overview of the LatAm Region
  • Adaptation from EU and differences within LatAm

Estefanny Da Silva

CMC requirements in Mexico
  • Pharmaceutical documentation
  • Additions and differences with regard to ICH requirements
  • Country specific requirements
  • Practical experiences (e.g. MAA, renewal, variations)
  • Avoiding typical mistakes in the dossier, common pitfalls
  • Lifecycle management: Post-approval changes: Standards in the ICH region, Additional and differing procedures/documentation in Mexico
  • Future trends
  • Practical activity

Coffee break


Ana Terra Dos Santos Macedo

CMC requirements in Brazil
Same content as lecture on Mexico.

Q&As


End of day I


Recap and outstanding questions of day I


Julieta Breton

CMC requirements in Argentina and Chile
  • Pharmaceutical documentation
  • Additions and differences with regard to ICH requirements
  • Country specific requirements
  • Practical experiences (e.g. MAA, renewal, variations)
  • Avoiding typical mistakes in the dossier, common pitfalls
  • Lifecycle management: Post-approval changes: Standards in the ICH region, Additional and differing procedures/documentation in Mexico
  • Future trends
  • Practical activity

Coffee break


Julieta Breton

CMC requirements in Peru
Same content as lecture on Argentina and Chile.

Estefanny Da Silva

CMC requirements in Colombia
Same content as lecture on Argentina and Chile.

Outstanding questions and conclusion


End of online seminar


More information

In-house seminars: Advanced training tailor-made!

You are looking for this topic for several employees?
We offer the right solution at your site or in virtual format!

We also offer this seminar as an in-house seminar.

Take advantage of the proven concepts of our open seminars and bring your employees to the same level of knowledge quickly and easily.

We will be happy to send you a non-binding offer.

Benefits of a FORUM Institut training course

FORUM Institut’s all-in-one training platform uses the latest teaching methods.
All our online training courses take place in the Learning Space, our holistic learning environment with many features that promote effective and sustainable learning.

  • Live and interactive learning on our Learning Space training platform
  • A platform with many features: events rooms, chat, course agendas and documents, surveys, workshop rooms and much more
  • Easy surveys with Slido
  • ‘Deluxe’ chat: group chats, one-to-one chats, one-to-one video chats
  • A central repository for documents and media
  • Other services and apps such as Padlet and Mentimeter available directly on the platform
  • The perfect marriage of teaching methods and technology
  • High level of interactivity with plenty of opportunity for questions
  • Continuous support throughout the event to ensure the most effective learning
  • Free technical pre-meeting to start off your training on the right foot

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.

This distinguishes our events

of 5 stars of all ratings from 2023

of 5 stars on Trustpilot = good

Recommendations

CTD: requirements for non-clinical/clinical modules and eCTD-readiness

Requirements for non-clinical/clinical content in the dossier: Are you a beginner in the field and would like to feel co...

18. - 19.09.2024, Online
Details

CMC dossier requirements for biologics: FDA vs EU

CMC requirements in the US: After having attended the seminar you will feel secure writing and maintaining the quality d...

16.10.2024, Online
Details

GxP-Regulated Archiving

Get practical expertise for the GMP, GLP and GCP-compliant archiving of relevant documents and the efficient integration...

24.09.2024, Online
Details
Masterclass China: Medical Device Marketing Authorisation for Advanced

Interested in establishing a strong presence in the Chinese medical devices market? Join our training to gain valuable i...

10. - 11.09.2024, Online
Details

Marketing Authorisation in Latin America

An online seminar to discuss real cases/challenges for marketing authorisation in Mexico, Argentina, Colombia, Peru, Chi...

26. - 27.09.2024, Online
Details

Go forward

Whitepaper: MA and lifecycle management in Japan

This whitepaper describes what you need to keep in mind when it comes to specific Japanese CMC requirements for marketin...

Details
Whitepaper: MA and lifecycle management in Japan
DEMO-Account

Try out our e-Learning programmes free of charge and without any obligation.

Details
DEMO Account
Our rating in 2023

More than 4,500 customers have rated our training courses. Thank you for awarding us 4.3 stars out of 5.

Details
Our rating in 2023