Luiz Levyrac

Q: What is Luiz Levy-rac email address?

Email Luiz Levy-rac at llevy08@gmail.com and llevyrac@emergo.marketing. This email is the most updated Luiz Levy-rac's email found in 2026.

Q: How to contact Luiz Levy-rac?

To contact Luiz Levy-rac send an email to llevy08@gmail.com or llevyrac@emergo.marketing. (updated on December 05, 2024)

Professor at Grupo IPOG | São Paulo, Brazil

About Luiz Levyrac

Luiz Levy-Rac currently serves as a Professor at Grupo IPOG, where he leverages his extensive expertise in Quality Assurance and Regulatory Affairs to educate and mentor the next generation of professionals in the medical device industry. His role involves designing and delivering comprehensive courses on Sanitary Regulation of Medical Devices and In Vitro Diagnostics, providing students with practical insights into the complex landscape of healthcare compliance. Luiz’s deep understanding of regulatory frameworks such as RDC 16/13, ISO 13485, ISO 9001, and CFR Part 820 enables him to translate industry standards into actionable knowledge, fostering a rigorous approach to quality management systems (QMS) and Good Manufacturing Practices (GMP).

In addition to his academic responsibilities, Luiz is actively involved in guiding companies through the intricacies of regulatory submissions, including ANVISA registration, FDA 510(k), UDI compliance, and CE Marking. His expertise in managing product lifecycle processes—from initial registration to post-market surveillance—ensures that organizations meet stringent regulatory requirements while maintaining high standards of quality and safety. Luiz’s proficiency in CAPA, TQM, and quality system implementation supports organizations in achieving continuous improvement and operational excellence.

Through his role at Grupo IPOG, Luiz not only imparts technical knowledge but also emphasizes the importance of strategic regulatory planning and compliance in the global medical device market. His industry-specific insights help students and professionals alike navigate the evolving regulatory landscape, ensuring that medical devices are safe, effective, and compliant with international standards.

Luiz Levyrac Work