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About Us

The IQ MPS is a collaboration of pharmaceutical and biotechnologies companies created as an Affiliate within the International Consortium for Innovation and Quality in Pharmaceutical Development (also known as the IQ Consortium) to provide a venue for appropriate cross-pharma collaboration and data sharing to facilitate the industry implementation and qualification of MPS models. The IQ Consortium is a leading science-focused, not-for-profit organization with a mission of advancing science and technology to augment the capability of member companies to develop transformational solutions that benefit patients, regulators and the broader R&D community (


The IQ MPS Affiliate is a not-for-profit organization devoted to raising awareness, advancing the science, and supporting the implementation of microphysiological systems in drug discovery. As such, the IQ MPS Affiliate does not collectively endorse microphysiological systems developers or their products. Presentations to the IQ MPS Affiliate are for awareness and information purposes. Individual IQ MPS Affiliate member organizations may engage external organizations as they see fit.


The Steering Committee provides strategic oversight of the initiative's portfolio and is the primary decision-making body for the IQ MPS Affiliate. The Steering Committee has representation from all member companies and acts on the recommendations of working groups and member companies to establish objectives, policies, and plans of action on a consensus basis.

The Executive Committee provides leadership and guidance in the management of the business and affairs of the consortium between meetings of the Steering Committee, implements strategic plans recommended by the Steering Committee, and provides general counsel and tactical advice in support of IQ MPS’s Working Groups.

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Rhiannon Hardwick, PhD, DABT

Past Chair (2024-2025)

Scientific Associate Director,

Bristol Myers Squibb

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Anna Kopec, PhD

Chair (2024-2025)

Director, Investigative Toxicology, Drug Safety R&D,


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Rhiannon David, PhD

Vice Chair (2024-2025)
Director of MPS, Safety Assessment,

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Kim Homan, PhD

Vice Chair Elect  (2024-2025)

Senior Director and Distinguished Scientist, Genentech Inc.

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Working Groups

Publish manuscripts outlining organ-specific industry requirements for MPS platforms.

Organotypic Manuscripts

Identify opportunities to engage with health authorities globally on topics related to MPS qualification.


Initiate near-term proof of concept study (POC) study for data sharing or prospective collaboration for qualifying MPS system(s) based on specific COUs.

Pilot Projects

Communicate industry perspective and build relationships with key MPS stakeholder to enhance the inclusion of industry priorities.

Strategic Partnerships and Communication

Landscape Survey

Conduct and analyze a survey benchmarking how pharmaceutical companies are currently using microphysiological models.


AbbVie, Inc.
Alnylam Pharmaceuticals, Inc.
Amgen, Inc
Astellas Pharma US, Inc.
Boehringer Ingelheim
Bristol-Myers Squibb Company
Daiichi Sankyo
Eisai, Inc.
Eli Lilly and Company

F. Hoffmann-La Roche

Genentech, Inc.

Janssen Pharmaceuticals, Inc.
Merck & Co., Inc.
Merck Healthcare KGaA
Novartis Pharmaceuticals Corporation

Novo Nordisk


Vertex Pharmaceuticals Incorporated


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