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Dec 24, 2025
  • Webinar

Driving Regulatory Readiness in Latin America

Explore some of the top compliance challenges companies face in Latin America, and steps organizations can take to mitigate risk.

colleen laconte

Date & Time

Starts

Dec 24, 2025 10:30am CST

Ends

11:00am CST

Location

Online

Language

English

Regulatory expectations across Latin America are evolving, making compliance more challenging for highly regulated industries such as pharmaceuticals, medical devices and biotech.

Join us for an informative 30-minute webinar, “Driving Regulatory Readiness in Latin America: Insights from ULTRUS™ ComplianceWire®. ” Our experts will shar e key strategies and actionable insights to help organizations modernize training, streamline documentation processes and prepare workforces to meet regulatory demands without relying on outdated systems or spreadsheets.

What you’ll learn:

  • Ways to streamline your compliance strategy using a comprehensive learning management system (LMS) platform with automated tools that support audit-readiness
  • Techniques for moni toring workforce development, including real-time tracking of employee certifications, progress and compliance metrics
  • Strategies for leveraging ComplianceWire® to proactively manage emerging regulations in Latin America through unified learning and auditing capabilities

Who should attend

This session is designed for professionals in:

  • Compliance and regulatory affairs
  • Risk management
  • Quality assurance and quality leadership
  • Procurement and supply chain
  • Supplier quality management
  • IT manager or leadership

Register today to explore region-specific compliance trends, challenges and innovations — and discover tools that empower quality and regulatory teams with confidence and clarity.

Speakers

Colleen Loconte, director and general manager, ComplianceWire® and Environmental, Health and Safety (EHS), brings over 35 years of expertise in life sciences, regulatory compliance and global quality management.

Sharon Brower, GXP industry subject matter expert, brings over 25 years of expertise in life sciences, regulatory compliance and global quality management.

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