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DIA 2019

DIA 2021 is Now Virtual!


Join Us Virtually in Latin America this Fall and Spring!

DIA is hosting back-to-back virtual events on Latin America in 2020 and another in 2021, and we want to see you there!

  • Latin America Medical Information and Communication Workshop

    November 4-5

    Organized and supported by medical information specialists in Latin America, local, regional, and global approaches to medical information and communication best practices will be shared and discussed at this workshop. Speakers will also focus on compliance topics, medical affairs services for patients, and regulatory affairs, as we holistically examine medical communication as it currently exists, and how it will continue to evolve.

  • Latin America Pharmacovigilance and Risk Management Strategies Workshop

    November 11-12

    DIA's Latin America Pharmacovigilance and Risk Management Strategies Workshop is the leading resource to discuss the current safety, pharmacovigilance, and risk management strategies landscape in Latin America. You'll gain insight from biopharmaceutical industry experts and global regulatory agencies on current policies and guidelines, and take part in collaborative, informative discussions centered on enhanced standardization of global compliance regulations.

  • Latin America Regulatory Affairs Conference

    February 22-23, 2021

    DIA brings you a symposium with interactive dynamics, where you will be engaged in discussions with key stakeholders influencing the advancement and implementation of regulatory convergence initiatives in Latin America. Join us to discuss multi-regional cooperation, global harmonization, and best practices related to Latin America’s regulatory landscape. Sessions will highlight regulatory approaches and good practices to ensure reliance in Latin American and strategic initiatives to improve collaboration and cooperation.

On-Demand Content Preview Webinars

Challenges of Producing a PBRER: Transition from PSUR to PBRER* 
Learn the main differences between the PSUR and the PBRER and analyze the challenges of producing such a document. You'll also examine the assessment of evidence, signal and risk evaluation, data in summary tabulations, exposure data, signal detection, missing information, and what to do when additional information is requested. Register here.
*This webinar will be in Portuguese with no English translation.

Medical Information in the Global Environment: Sharing the Experience on How to Build Global MI Teams and Processes 
Discuss how the medical information area is growing and evolving and aligned to trending global structures in the pharmaceutical industry. The webinar will provide real case scenarios on how teams are growing and being built, and will also share the challenges involved in harmonization of processes around the globe. Register here.

On Demand: Brazil – Compliance: What is the Balance Between Medical Affairs Services and Customers?*
*This webinar is in Portuguese with no English translation.

Session Recording: Regulatory Update in Approving Biosimilars and Approach to Interchangeability


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