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Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
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Appendix D

Registered Attendees

Joe Alper

Consultant

Salomon Amar

New York Medical College

Rachael Anatol

U.S. Food and Drug Administration

Judith Arcidiacono

U.S. Food and Drug Administration

Gillian Armstrong

PACT

Chris Ballas

WuXi AppTec

Steven Bauer

U.S. Food and Drug Administration

Steven Becker

National Eye Institute

Kimberly Beer

Christopher & Dana Reeve Foundation

Kapil Bharti

National Eye Institute

Sarindr Bhumiratana

EpiBone Inc.

Catherine Bollard

International Society for Cellular Therapy

Tom Bollenbach

Advanced Regenerative Manufacturing Institute

Lizbet Boroughs

Association of American Universities

Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×

Melissa Carl

American Society of Mechanical Engineers

Preethi Chander

National Institute of Dental and Craniofacial Research

R. Alta Charo

University of Wisconsin Law School

Gray Chynoweth

Advanced Regenerative Manufacturing Institute

Michelle Cortes

National Institute of Dental and Craniofacial Research

Robert Deans

BlueRock Therapeutics

Cynthia Dunbar

American Society of Gene and Cell Therapy

Donald Fink

U.S. Food and Drug Administration

Ellen Gadbois

National Institutes of Health

John Gardenier

Independent

Turkan Gardenier

Pragmatica Corporation

Lindsay Garvin

National Heart, Lung, and Blood Institute

Adrian Gee

Center for Cell and Gene Therapy, Baylor College of Medicine

Larry Goldstein

University of California, San Diego

Daniel Gossett

National Institutes of Health

Joseph Griffin

MassMEP

Rachel Haddock

GlaxoSmithKline

Patrick Hanley

International Society for Cellular Therapy

Joshua Hare

University of Miami

Brian Harvey

Global Liver Institute

Daniel Hayes

The Pennsylvania State University

Susan Howley

Christopher & Dana Reeve Foundation

Deborah Hursh

U.S. Food and Drug Administration

Laarni Ibenana

The Emmes Corporation

Shekhar Jha

National Institutes of Health

Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×

Ping Jin

National Institutes of Health

Naynesh Kamani

American Association of Blood Banks

Dean Kamen

DEKA Research & Development

Linda Kelley

Moffitt Cancer Center

Walter Koroshetz

National Institutes of Health

Paul Kotturi

Pacific Biosciences

Audrey Kusiak

Department of Veterans Affairs

Larissa Lapteva

U.S. Food and Drug Administration

Cato Laurencin

University of Connecticut

Timothy LaVaute

National Institute of Neurological Disorders and Stroke

Anh Le

University of Pennsylvania

Bruce Levine

University of Pennsylvania

Rachel Levinson

Arizona State University

Jinhua Lu

U.S. Food and Drug Administration

Erin Luetkemeier

National Institutes of Health

Martha Lundberg

National Heart, Lung, and Blood Institute

Terry Magnuson

University of North Carolina at Chapel Hill

Keith March

Indiana University School of Medicine

Kurt Marek

National Heart, Lung, and Blood Institute

Ross Marklein

U.S. Food and Drug Administration

Nancy Markovitz

Diamond Pharma Services, Inc.

Jessica Mazerik

National Eye Institute

Robert McBurney

Accelerated Cure Project for Multiple Sclerosis

Richard McFarland

Advanced Regenerative Manufacturing Institute

Mark McMenemy

MassMEP

Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×

Kaye Meier

International Society for Stem Cell Research

Phyllis Mitchell

National Heart, Lung, and Blood Institute

Jason Moore

Smithfield Foods

Kirsten Moore

The Pew Charitable Trusts

Malcolm Moos

U.S. Food and Drug Administration

Jack Mosher

International Society for Stem Cell Research

Melissa Moss

Biomedical Engineering, University of South Carolina

Eleanor Nicoll

American Society for Reproductive Medicine

Laura Niklason

Department of Anesthesia, Yale University

Kim O’Connor

Tulane University

Steven Oh

U.S. Food and Drug Administration

David Owens

National Institute of Neurological Disorders and Stroke

Diana Pankevich

Pfizer Inc.

Duanqing Pei

Guangzhou Institutes of Biomedicine and Health, CAS

Thomas Petersen

United Therapeutics

Russell Pirlo

BioFabUSA

Anne Plant

National Institute of Standards and Technology

Nicole Polinski

The Michael J. Fox Foundation for Parkinson’s Research

Kristy Pottol

U.S. Army Medical Materiel Development Activity

Libbie Prescott

National Defense University

Robert Preti

PCT Cell Therapy Services, LLC

Jiaqiang Ren

National Institutes of Health

James Richardson

Foundation Fighting Blindness

Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×

Rod Rietze

Novartis Institutes for Biomedical Research

Joseph Rimsa

TauTona Group Research and Development Company, L.L.C.

Isabelle Rivière

Memorial Sloan Kettering Cancer Center

Kelley Rogers

Office of Advanced Manufacturing, National Institutes of Health

Heather Rooke

International Society for Stem Cell Research

Krishnendu Roy

Georgia Institute of Technology

Beth Russell

Alder Data-Driven Solutions

Stephanie Saddic

GlaxoSmithKline

Krishanu Saha

University of Wisconsin–Madison

Sumona Sarkar

National Institute of Standards and Technology

Stephanie Scarmo

The Pew Charitable Trusts

Basant Sharma

Janssen Research & Development

Jay Siegel

Johnson & Johnson

Ilyas Singec

National Center for Advancing Translational Sciences

Aparna Singh

National Institutes of Health

Martha Somerman

National Institute of Dental and Craniofacial Research

Courtney Stanton

Smithfield Foods

Binil Starly

North Carolina State University

Sohel Talib

California Institute for Regenerative Medicine

William Tente

Humacyte

Sharon Terry

Genetic Alliance

John Thomas

National Heart, Lung, and Blood Institute

Zehra Tosun

U.S. Food and Drug Administration

Katherine Tsokas

Janssen Research & Development

Philip Vanek

GE Healthcare

Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×

Jason Wan

National Institute of Dental and Craniofacial Research

Fei Wang

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Rachel Weissman

Research!America

Anthony Welch

National Cancer Institute

Lisbeth Welniak

National Institutes of Health

Jason Wertheim

Northwestern University

Angela Whatley

U.S. Food and Drug Administration

Celia Witten

U.S. Food and Drug Administration

Michael Yaffe

The New York Stem Cell Foundation

Shaomian Yao

Louisiana State University

Carolyn Yong

U.S. Food and Drug Administration

Michael Yost

Medical University of South Carolina

Jiwen Zhang

GE Healthcare

Yuji Zhang

University of Maryland Baltimore

Claudia Zylberberg

Akron Biotech

Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×
Page 99
Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×
Page 100
Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×
Page 101
Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×
Page 102
Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×
Page 103
Suggested Citation:"Appendix D: Registered Attendees." National Academies of Sciences, Engineering, and Medicine. 2017. Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies: Proceedings of a Workshop. Washington, DC: The National Academies Press. doi: 10.17226/24913.
×
Page 104
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On June 26, 2017, the Forum on Regenerative Medicine hosted a public workshop in Washington, DC, titled Navigating the Manufacturing Process and Ensuring the Quality of Regenerative Medicine Therapies in order to examine and discuss the challenges, opportunities, and best practices associated with defining and measuring the quality of cell and tissue products and raw materials in the research and manufacturing of regenerative medicine therapies. The goal of the workshop was to learn from existing examples of the manufacturing of early-generation regenerative medicine products and to address how progress could be made in identifying and measuring critical quality attributes. The workshop also addressed the challenges of designing and adhering to standards as a way of helping those who are working to scale up processes and techniques from a research laboratory to the manufacturing environment. This publication summarizes the presentations and discussions from the workshop.

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