The Biosimilars LatAm – Mexico 2022 forum’s main focus is The Collaborative Approach which is priorly aimed at harmonizing the legal frameworks that are applicable to biosimilar drugs.

The goal is to seek and strengthen all prescription and access processes of these treatments in order to help the patients in the region.

Collaborative approaches in general, require a multidisciplinary effort and therefore all sessions presented during this forum, will provide you with a wide scope of the current status and efforts that have been made towards the improvement of the public health sector in Mexico and Latin America.

Featured panels:

– Regulatory
– Quality & Production
– Commercialization
– Innovation & Competition


Who will
you meet?


More than:









Service Providers

Government Agencies

Industry Executives from Latam

From these areas:

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

Speaker Board

Program at a Glance

Collaborative: Reference Authorities' Updates and Actions Towards Regulation for Biosimilars

Stay on top of the newest regulations and tendencies led by reference authorities on biosimilars regulatory frameworks

Quality and Integrity of Biopharmaceutical Products Within Production Processes

How to ensure the safety of biotech products within Production processes? Experts sharing their point of view

Commercial Measures for Biosimilars in the LatAm Markets

Commercial strategies and market dinamycs to ensure the promotionof biosimilars uptake in Mexico and LatAm

Global innovation and Competitiveness in Pharmaceuticals: Biosimilars Case Study

How to innovate in the biosimilars industry and highly competitive markets?

Full programme in the PDF Agenda

Download Agenda



We are a vibrant science and technology company. Science is at the heart of everything we do, it drives the discoveries we make and the technologies we create. For more than 350 years, curiosity has been driving us to deliver excellence to patients and customers – and to imagine the future.


Agilent is a leader in life sciences, diagnostics and applied chemical markets. The company provides laboratories worldwide with instruments, services, consumables, applications and expertise, enabling customers to gain the insights they seek. Agilent’s expertise and trusted collaboration give them the highest confidence in our solutions.


Pall associates around the world are unified by a singular drive: to solve our customers’ biggest filtration, separation and purification challenges. And, in doing so, advance health, safety and environmentally responsible technologies. 

Our industry-leading technologies and solutions are at work in countless applications, safeguarding health, protecting critical operating assets, improving product quality, and minimizing emissions and waste. 

Our Life Sciences and Industrial teams bring focused expertise to a diverse range of customers across multiple industries, including biotechnology, pharmaceutical, medical, food and beverage, laboratory, microelectronics, aerospace, fuels, petrochemical, chemical, automotive and power generation .


Cytiva is a global provider of technologies and services that help advance and accelerate the development and production of therapeutic products. Promoting training, speed and efficiency for research and production workflows, allowing the delivery of innovative medicines to patients.



We develop alliances with pharmaceutical companies, using Terumo technology to develop, manufacture and supply solutions to injectable drug delivery challenges. We pride ourselves on offering a portfolio of products and services for the pharmaceutical industry. By anticipating trends and maintaining a constant dialogue, we provide a first class customer experience.


Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.


With 60+ dedicated scientists and support personal, UDIBI is a third-party laboratory authorized by the Mexican Regulatory Agency (COFEPRIS) to conduct analytical services for the pharmaceutical and medical devices industries. We also provide consulting services on antibody engineering and development of antibody-based therapeutics. With the support from government and private investment we have developed a portfolio of biotherapeutics that includes a product in the market and several therapeutic antibodies in diverse phases of discovery, optimization and preclinical development. In response to COVID-19 pandemic, UDIBI developed and commercializes the only 100% Mexican diagnostic kit to detect anti-SARS-CoV-2 antibodies with approval by COFEPRIS for commercialization in Mexico.

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