Image
Image

Unlocking Opportunities in Latin America: Trends, Membership, and Annual Meeting Insights

Wednesday, July 24, 2024 at 10:00AM ET

Image
In this Webinar…

Join us for a complimentary dynamic 75-minute webinar delving into the upcoming DIA Latin America Annual Meeting and the extensive membership opportunities for stakeholders in the region. Our distinguished presenters will unveil emerging trends in LATAM, share their experiences as DIA members, and emphasize the significant benefits of DIA membership.


Learning Objectives:

Designed to ignite engagement, collaboration, and knowledge-sharing among Latin American stakeholders, this session offers a unique deep-dive into the full potential of DIA membership.

Presenters:

  • Tamei Elliott, MS 
    Associate Director, Scientific Programs, DIA, United States
  • Leonardo Semprun, PharmD 
    Global Regulatory Policy Lead-LatAm, MSD, Panama
  • Maria Antonieta (Tony) Roman, MPharm 
    Head Regulatory Policy Emerging Markets LATAM, Novartis, Mexico
  • Raphael Elmadjian Pareschi, PharmD, MBA 
    Patient Safety Lead/ Head of Pharmacovigilance Brazil, Roche, Brazil
  • Barbara Nardi, PharmD 
    Global Director - Medical Communications, Thermo Fisher Scientific, Brazil
  • Clare Bedford 
    Member Engagement & Operations Manager, DIA, United States
Image
Sign up below to register!

Lorem ipsum dolor sit amet consectetur adipisicing elit. Odit vero harum distinctio autem?

Lorem ipsum dolor sit amet consectetur adipisicing elit. Quam laborum reprehenderit amet in rerum id eum harum qui quos. A est consequatur reprehenderit necessitatibus repudiandae quia harum dolorum praesentium temporibus?

Form Title

Who Should Attend?

  • Academia
  • Benefit-Risk Assessment and Communication
  • Clinical Research and Development
  • Clinical Operations
  • CROs/Vendors
  • Document Management/eSubmissions
  • Drug Regulation
  • Drug Safety/Pharmacovigilance
  • Field Medical
  • Global Submission/Project Management
  • Government Affairs
  • Manufacturing
  • Medical and Scientific Affairs
  • Medical Call Center Environment
  • Medical Communications
  • Medical Information
  • Medical Product Safety Assessment
  • Medical Science Liaisons
  • Medical Writing
  • Pharmacoepidemiology
  • Policy and Intelligence
  • Post-Market Studies
  • Quality Assurance and Compliance
  • Real-World Evidence
  • Regulatory Agencies
  • Regulatory Affairs, Operations, and Strategy
  • Research and Development
  • Risk Management, including Risk Evaluation and Mitigation Strategies (REMS)
  • Strategic Sourcing/Planning

Video Title Lorem ipsum dolor sit amet.