Biosimilars LatAm – Mexico 2025
Designed to advance greater access to biosimilars in Mexico, this forum convenes top decision-makers from manufacturers, regulators, and healthcare providers. Featuring dynamic presentations, interactive panels, and networking spaces, the event delves into policy reforms, investment strategies, and environmental sustainability in biosimilar production. The forum also explores innovative regulatory approaches and public-private collaborations aimed at accelerating approvals and improving affordability, reinforcing Mexico’s competitive position in the biotechnology sector.
Key Objectives:
– Evaluate policies to expand biosimilar access for vulnerable populations and redistribute healthcare savings to improve equity.
– Analyze strategies to position Mexico as a competitive destination for biotechnology investments, exploring regulatory and market opportunities.
– Discuss environmental challenges in biosimilar production and explore solutions for sustainable manufacturing practices aligned with global goals.
– Explore strategies to accelerate biosimilar approvals in Mexico, maintaining safety and efficacy standards while fostering public-private partnerships.
Who will
you meet?
More than:
Participants
Companies
HCPs
Patients
Academy
Investors
Institutions
Associations
Service Providers
Government Agencies
Industry Executives from Latam
- Biosimilars
- Biobetters
- Biotechnology
- Biotherapeutics
- Analytical science
- Regulatory compliance
- Quality Control
- Clinical immunology
- Scientific Affairs
- Pharmacovigilance
- Research
- Regulatory
- Business Development
- Marketing
Plan Your 1-to-1 Meetings with JackLeckerman WebApp
Speaker Board
Enrique Martinez Moreno
General Director & Founder
José Luis Garcia Rodríguez
President & Founder
José Antonio Sandoval Rubio
Project Coordinator E1
Juan Jose Giraldo Navia
Country Manager Mexico
Ricardo Del Olmo Hidalgo
Executive Director
Becky Kimberley Viera Juárez
Development and Research Project Specialist
Mayra Guadalupe Quiñonez Alvarado
Head of Bioanalytical Control
Adriana Valdés Campos
Corporate Affairs and Public Relations Director for Latin America
Marcos Iván González Jaime
Field Application Specialist
Baiba Cabovska
Biopharma Market Development Manager
Beatriz Chebly
Head of Regulatory Affairs
Eduardo Ortí
Manager of Biotechnological Projects
Oyuki Sekisaka Pérez
Senior Manager of Regulatory Affairs
Pablo de Felipe
Head of Service – Virology
Sarem Hailemariam
Platform Development Specialist
Patrícia Guimarães
Regional Sales Manager Latam
Peter Gurske
Managing Director
Edgar Vazquez Ramos
Field Application Scientist
Mabel Rodriguez
Operational Head of the Molecule and Drug Analysis Laboratory
Pablo Alberto Quiroga Adame
Project Director
Juan de Villafranca
CEO
Tonatiuh Cortes Esquivel
Sr Strategic Project Manager
Irma Garcia Morales
Regional Compliance Head Mexico – LatAm
Cristina Ausin
Scientific Reviewer
Mayra Galindo Leal
Director
Jaime Uribe Wiechers
General Manager
Fernando Fon
Executive Director
Program at a Glance
Next-Generation Biosimilar Manufacturing: Efficiency, Quality, and Innovation
Highlight technological and process innovations enhancing efficiency, quality, and sustainability in next-generation biosimilar manufacturing.
Nearshoring in Mexico: Opportunities for the Pharmaceutical Industry
Analyze how relocating supply chains to Mexico boosts pharmaceutical industry growth and competitiveness.
Biosimilar European Regulatory Updates
EMA’s ongoing work on the Reflection Paper for a tailored clinical approach in biosimilar development, which is reassessing the role of Comparative Efficacy Studies (CES) in biosimilar comparability exercises.
Recent FDA Developments in Biosimilar Regulation
Technology and Innovation in Biosimilar Manufacturing: Equipment, Efficiency, and Future Bioprocessing
Explore the latest technological advancements and innovative approaches in biosimilar manufacturing, highlighting how state-of-the-art equipment, process optimization, and next-generation bioprocessing are enhancing efficiency, quality, and scalability to strengthen global competitiveness.
Attracting Investments for Biosimilars: A Roadmap for Mexico
This panel will analyze strategies to position Mexico as a competitive destination for investments in biotechnology. Panelists will discuss investment trends, market opportunities, and the role of regulation in fostering a favorable business environment.
Strengthening Competitiveness: Overcoming Barriers in the Mexican Biosimilars Market
Analyze how intellectual property (IP) protection and collaborative innovation ecosystems contribute to strengthening business readiness and competitiveness. The session aims to highlight best practices that enable companies to transform knowledge into market value, foster partnerships, and create sustainable growth within an innovation-driven economy.
Access and Equity: Ensuring Biosimilars Reach Those Who Need Them Most
This panel will evaluate policies for expanding access to biosimilars among vulnerable populations, discussing effective frameworks for redistributing healthcare savings to improve equity.
Regulatory Innovation for Faster Biosimilar Approvals in Mexico
This panel will explore innovative strategies to reduce the time required for biosimilar approvals in Mexico while maintaining safety and efficacy standards. Discussions will include global best practices, necessary policy changes, and the role of public-private partnerships.
Full Programme in the PDF Agenda
Download Agenda
Exclusive Workshop for Branded Drug Manufacturers
November 10 | Camino Real Polanco, Mexico City
Learn how to detect nitrosamines and antibodies using advanced analytical platforms (TQ and QTOF) in a practical, hands-on format.
A unique opportunity to deepen your understanding of biopharmaceutical quality control using the latest technological developments.
Limited to 15 participants – lunch included.
Personalized Micro-Consulting for Forum Attendees
As part of the exclusive benefits of Biosimilars LatAm – Mexico 2025, all forum participants will have access to a complimentary one-on-one micro-consulting session with a Certified Expert Consultant from JackLeckerman. An invaluable opportunity to align your professional and business objectives with practical strategies that drive growth in the sector.
This benefit is designed to ensure every attendee gains maximum value from their forum participation.
Sessions will take place during the scheduled networking breaks.
Sponsors
Media Partners
Photo Gallery from Previous Events
Testimonials
Previous Forums
How to attend?
Keep me updated










