content contributor liza gordillo

Liza Gordillo, MS

KLS Martin Group

With nearly 15 years of experience in the regulatory field, Liza Gordillo serves as Regulatory Affairs Project Manager at KLS Martin Group. Currently, she authors 510(k) submissions while collaborating with cross-functional teams in the design and development of medical devices. Prior to joining KLS Martin, Liza was an IRB Regulatory Analyst for the University of Miami’s Institutional Review Board. At UM, she led study teams through the IRB process by providing support in the review of informed consent and ensuring submissions met IRB requirements for the protection of human subjects. Liza later joined Stryker as a Senior Regulatory Affairs Specialist in the division of robotic surgery.

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Understanding ISO 14155:2020 Revisions


This webinar examines the new ISO 14155 medical device standard while exploring its implications for sponsors and investigators.

Understanding ISO 14155:2020 Revisions