Biosimilars Mexico 2018 Forum

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Discussions

Interactive discussion with regulatory experts striving for consolidated regulation

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Updates
All stakeholders in one place
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Advices

Ask HCPs and Patients how to develop your strategies

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Fresh views

C-level executive outlook on the future of Biosimilars in LATAM

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Summary

The regulation of similar bio-therapeutic products varies widely among the different Latin American countries. While some of them are yet to introduce their own regulation, others — like Brazil and Mexico — have opened ways to cheaper, complex and safe biological treatment for patients. However, many things need improving and a lot of experience is still necessary to develop a mature LATAM Biosimilars Market.

Biosimilars Forum 2017 is a unique and effective meeting point to share the information and experience Latin America’s Pharmaceutical Industry needs to develop a dynamic and thriving biosimilars market.Join us in Mexico and trigger a quantum leap in Latin American Healthcare!

Who will
you meet?

More than:

 

0
Participants
0
Companies

Directors

VP's

CEO's

COO's

Bio-technologists

Managing Directors

Managers and Specialists

From these areas:

  • Biosimilars
  • Biobetters
  • Biotechnology
  • Biotherapeutics
  • Analytical science
  • Regulatory compliance
  • Quality Control
  • Clinical immunology
  • Scientific Affairs
  • Pharmacovigilance

Highlights from 2017

Programme at a Glance

LATAM Regulations Update
By Anvisa and Coferpis
How Biosimilars are being developed in Latam
Clinical Trials required for Biosimilars?
Biosimilars, The Mexican Industry Approach
Clinical Research and the Registration of Biosimilars
Interview: Industry Leaders and Their Strategy to Increase Biosimilar’s Access in the Region
Full programme in the PDF Agenda

How to attend

Biosimilars Latam 2018 Forum

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