QA Lion
QA Lion

Melissa Finocchio

QA Lion - The Lion that Guards

Melissa Finocchio is a regulatory and quality leader with over 25 years of experience driving innovation and compliance in in vitro diagnostics and medical devices. Her experience spans the full product lifecycle – from development to post-market – across products ranging from rapid tests to AI-driven software for Next Generation Sequencing and companion diagnostics.

An executive leader, Melissa is passionate about translating complex regulatory requirements into practical, business-enabling solutions. She has led global teams across the United States, Europe, and beyond, bringing first-hand insights into international regulatory strategy, cross-cultural collaboration, and operational excellence. Melissa advocates for regulatory and quality functions not just as compliance necessities, but as strategic drivers of innovation, efficiency, and patient impact.

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QA Lion
QA Lion

Melissa Finocchio

QA Lion - The Lion that Guards

Melissa Finocchio is a regulatory and quality leader with over 25 years driving innovation and compliance in in vitro diagnostics and medical devices. Her experience spans the full product lifecycle – from development to post-market – across products ranging from rapid tests to AI-driven software for Next Generation Sequencing and companion diagnostics.

An executive leader, Melissa is passionate about translating complex regulatory requirements into practical, business-enabling solutions. She has led global teams across the United States, Europe, and beyond, bringing first-hand insights into international regulatory strategy, cross-cultural collaboration, and operational excellence. Melissa advocates for regulatory and quality functions not just as compliance necessities, but as strategic drivers of innovation, efficiency, and patient impact.

Image

Melissa Finocchio

QA Lion - The Lion that Guards

QA Lion
QA Lion

Melissa Finocchio is a regulatory and quality leader with over 25 years driving innovation and compliance in in vitro diagnostics and medical devices. Her experience spans the full product lifecycle – from development to post-market – across products ranging from rapid tests to AI-driven software for Next Generation Sequencing and companion diagnostics.

An executive leader, Melissa is passionate about translating complex regulatory requirements into practical, business-enabling solutions. She has led global teams across the United States, Europe, and beyond, bringing first-hand insights into international regulatory strategy, cross-cultural collaboration, and operational excellence. Melissa advocates for regulatory and quality functions not just as compliance necessities, but as strategic drivers of innovation, efficiency, and patient impact.

Image
QA Lion

Melissa Finocchio

QA Lion - The Lion that Guards

QA Lion

Melissa Finocchio is a regulatory and quality leader with over 25 years driving innovation and compliance in in vitro diagnostics and medical devices. Her experience spans the full product lifecycle – from development to post-market – across products ranging from rapid tests to AI-driven software for Next Generation Sequencing and companion diagnostics.

An executive leader, Melissa is passionate about translating complex regulatory requirements into practical, business-enabling solutions. She has led global teams across the United States, Europe, and beyond, bringing first-hand insights into international regulatory strategy, cross-cultural collaboration, and operational excellence. Melissa advocates for regulatory and quality functions not just as compliance necessities, but as strategic drivers of innovation, efficiency, and patient impact.

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How we can help

Expertise

ISO 13485 - Medical Devices - Quality Management Systems 

ISO 9001 - Quality Management Systems

ISO 14971 - Risk Management for Medical Devices

ISO 27001 - Information Security Management System

ISO 18113 - IVD Labeling

IEC 62304 - Medical Device Software Product Lifecycle

EU 2017/746 (IVDR) & EU 2017/745 (MDR)

Medical Device Single Audit Program (MDSAP)

Unique Device Identifier (UDI)

FDA

  • 21 CFR 11 - electronic records and electronic signatures
  • 21 CFR 809 - In vitro diagnostic products for human use
  • 21 CFR 820 - Quality System Regulation

Support Throughout the Product Life Cycle

Support Throughout the Product Life Cycle

Support Throughout the Product Life Cycle

Support Throughout the Product Life Cycle