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Project

Medical Device Initiative

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Pew Comments on the Unique Device Identification System Issue Brief

Pew Comments on the Unique Device Identification System

Nov 8, 2012

 Pew’s Medical Device Initiative, along with the American Heart Association and Trust for America’s Health, submitted comments to the U.S. Food and Drug Administration (FDA) regarding its proposed rule for a unique device identification (UDI) system for medical devices. More
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Comments on Stage 3 of the the Meaningful Use of Health Information Technology

Issue Brief
  • Jan 15, 2013

In comments to the Office of the National Coordinator for Health Information Technology (ONC), the American College of Cardiology and The Pew Charitable Trusts urge the ONC to incorporate medical device identifiers developed under the FDA’s unique device identification (UDI) system into both electronic health record (EHR) certification criteria and Stage 3 meaningful use (MU) objectives. More

Issue Brief

Comments on the Health Information Technology Patient Safety Action and Surveillance Plan

Issue Brief
  • Feb 5, 2013

In comments to the Office of the National Coordinator for Health Information Technology (ONC), the American College of Cardiology, Consumers Union, the National Women's Health Network, the National Research Center for Women and Families, the Trust for America's Health, and The Pew Charitable Trusts urge the ONC to promote adoption of the unique device identification (UDI) system for medical devices to improve the safety of medical care.

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Issue Brief

Expert Profile: Allan Coukell

Video
  • Feb 17, 2012

Allan Coukell, Deputy Director, Medical Programs

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Video

Expert Profile: Josh Rising

Video
  • Sep 24, 2012

Josh Rising, Project Director, Medical Device Initiative More

Video

Facilitating Medical Device Innovation: De Novo Reform

Issue Brief
  • Jun 22, 2012

The de novo process as it exists now is not achieving its purpose of streamlining the path to move new devices onto the marketplace and has instead added unnecessary and time-consuming requirements. More

Issue Brief

Improving Medical Device Safety Through Better Surveillance

Issue Brief
  • Jun 22, 2012

In 2008, the Food and Drug Administration (FDA) launched the Sentinel Initiative, a national electronic system designed to “track the safety of drugs, biologics, and medical devices once they reach the market.” By proactively monitoring data from electronic health records and other sources rather than relying on spontaneous reporting from manufacturers and health care providers, the Sentinel system can more quickly identify safety issues.

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Issue Brief

Letter From New Democrat Health Care Task Force to FDA on Unique Device Identification System

Issue Brief
  • Apr 25, 2013

The three co-chairs of the New Democrat Health Care task Force – Reps. Allyson Schwartz, Kurt Schrader and Bill Owens – sent FDA a letter inquiring about the status of the agency’s final regulations to establish a unique device identifier (UDI) system and database.

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Issue Brief

Letter from Pew and Premier to the OMB on Unique Device Identifier Rule

Issue Brief
  • Jul 8, 2013

The Pew Charitable Trusts and the Premier healthcare alliance sent the White House Office of Management and Budget a letter regarding the review of a Food and Drug Administration rule to establish a unique device identifier (UDI) system. Given the importance of this new device identification system to improve patient care and the missed statutory deadline, in this correspondence Josh Rising of Pew and Blair Childs of Premier strongly urged the Director of the Office of Management and Budget (OMB) to promptly complete review of the UDI final rule.

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Issue Brief

Letter from Pew to FDA on Postmarket Surveillance Plan

Issue Brief
  • May 30, 2013

FDA recently updated the national medical device postmarket surveillance plan – listing device identification and registries as the cornerstones for effective product monitoring. In this letter, medical devices director Josh Rising applauds the agency for making unique device identifiers and registries central to this plan.
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Issue Brief

Letter from Pew: Release of the Unique Device Identifier Final Rule

Issue Brief
  • Jun 27, 2013

A letter from Josh Rising — director of Pew's Medical Device Initiative — to The White House Office of Management and Budget, requesting a speedy review of regulations to develop a unique device identifier (UDI) system. More

Issue Brief

Letter from Pew: Updates on the Unique Device Identifier System

Issue Brief
  • Jun 18, 2013

A letter from Josh Rising, director of Pew's Medical Device Initiative, about updates on the unique device identifier system.

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Issue Brief

National Public Health Week

Other Resource
  • Mar 29, 2013

This year's celebration of National Public Health Week (NPHW) focuses on the theme, "Public Health is ROI: Save Lives, Save Money." Join us in recognizing the work of Pew's Health Initiatives. More

Other Resource

Pew Comments on Draft Recommendations for Meaningful Use, Stage 3

Issue Brief
  • Apr 4, 2013

The Pew Charitable Trusts submitted comments on preliminary recommendations regarding Stage 3 meaningful use objectives and standards for electronic health records (EHRs) to the Office of the National Coordinator for Health Information Technology. These comments follow remarks at recent meetings of the Health Information Technology (HIT) Policy Committee and HIT Standards Committee.

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Issue Brief

Protecting Human Health Through Better Device Tracking

Other Resource
  • May 3, 2013

The U.S. Food and Drug Administration (FDA) has issued a proposed rule that would require manufacturers of medical devices, with certain exceptions, to place a unique identifier on the label of medical devices. Some medical devices would also need to be directly marked with the unique identifier.

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Other Resource

Seeking Better and Safer Medical Devices

Other Resource
  • Nov 27, 2012

Medical devices range from common iteams such as stethoscopes to more complex products such as pacemakers and heart stents. The Medical Device Initiative project seeks to improve the tracking of medical device safety and to foster innovation that benefits patients. Project Director Josh Rising has a personal connection to the value of medical devices and he explains the importance of the Initiative and the goals of the program.

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