Webinar Features
Medical Device Registration in LATAM countries Brazil and Mexico
Understand the regulatory pathways for market access, crucial for informed decision-making and compliance in Brazil and Mexico.
Format
On-Demand Webinar
Level
Basic
Trainer
Patrícia Da Silva Perez and Olena Hoi
Exam
Certificate of Participation included
Duration
1 hour
Price
Free
Comprehensive Regulatory Expertise
Watch this On-Demand webinar to learn more about the regulatory framework in Latin American countries Brazil and Mexico, presented by our regulatory affairs associates around the world.
Watch on-demand webinars at your convenience, allowing you to fit learning into your schedule without missing essential information.
Flexible Viewing
Gain insights from industry experts and stay updated on the latest trends and regulations without the need to attend live sessions.
Access to Expertise
Meet the Trainer
Patrícia Da Silva Perez
Patrícia da Silva Perez, PhD, is an expert in biocompatibility, clinical evaluations, and regulatory affairs, with over five years of experience in the medical device industry, particularly in the dental field, and she is now part of Qserve's Clinical Operations unit.
Meet the Trainer
Olena Hoi
Olena is a seasoned Quality and Regulatory Affairs Consultant at Qserve Group with extensive experience in managing Quality Management Systems, conducting audits, and authoring regulatory submissions for high-risk medical devices across global markets, particularly in the EU under MDR and MDD regulations.
