Clean Production Action developed the GreenScreen Certified Standard for Medical Supplies & Devices in consultation with a diverse group of stakeholders, including manufacturers, purchasers, and external scientific experts from consulting firms, government, academic, and non-profit organizations.

This effort would not have been possible without the help of the technical peer reviewers and key contributors, who devoted their time and consider-able expertise to the development of this standard. Providing advice and feedback during technical peer review shall in no way be construed as support for the final standard. The key contributors ultimately take respon-sibility for all content and any flaws or errors contained herein. In producing the final standard, we thank Ellen Goldberg, Kayla Williams, and Beverley Thorpe of Clean Production Action for their efforts in developing legal terms of use, and communication and website resources necessary to implement and launch the certification program.

Key Contributors

Shari Franjevic, GreenScreen Program Manager,
Clean Production Action
 
Amy Hunsicker, Consultant to Clean
Production Action
 
Mark S. Rossi, PhD, Executive Director,
Clean Production Action
 

Technical Peer Reviewers 

Carol Summers, NewGen Surgical
 
Elizabeth Eldridge, Kaiser Permanente
 
Hannah Anderson, Medline Industries, Inc.
 
Joel Sigler, Kaiser Permanente
 
Kyle Tafuri, Hackensack Meridian
 
Maria Nagel, MD, University of
Colorado Medical School
 
Michael Turturro, Medline Industries, Inc.
 
Monica Nakielski, Blue Cross Blue Shield
of Massachusetts
 
Paul Ciccone, WilMarc Medical
 
Rob Chase, NewGen Surgical
 
Ron Hart, PhD, Former Executive Director,
National Center for Toxicology Research
at FDA
 
Ted Schettler, MD, MPH, Science and
Environmental Health Network (SEHN)
 
Yoav Einy, Vizient

Share: