COVID-19 and access to medical products : implications of Section 301 tariffs /

COVID-19--2021 : hearing before the Committee on Homeland Security and Governmental Affairs and the Committee on Rules and Administration, United States Senate, One Hundred Seventeenth Congress, first session: Preparedness for COVID-19: the initial pandemic response and lessons learned, April 14, 2021 and COVID-19 Part II: evaluating the medical supply chain and pandemic response gaps, May 19, 2021.
Published: (2022)

VA acquisition management: supply chain management and COVID-19 response : testimony before the Committee on Veterans Affairs, U.S. Senate /
by: Oakley, Shelby, S.
Published: (2020)

Classification names for medical devices and in vitro diagnostic products /
Published: (1991)

Medical device regulation : the FDA's neglected child : an oversight report on FDA implementation of the Medical Device Amendments of 1976 : report of the Subcommittee on Oversight and Investigations of the Committee on Energy and Commerce, U.S. House of Representatives.
Published: (1983)

Medical device development : regulation and law /
by: Kahan, Jonathan S.
Published: (2009)

Medical device register.
Published: (1981)

Medical devices and equipment : competitive conditions affecting U.S. trade in Japan and other principal foreign markets.
Published: (2007)

COVID-19 contracting: Indian Health Service used flexibilities to meet increased medical supply needs : report to congressional addressees.
Published: (2021)

Federal policies and the medical devices industry /
Published: (1984)

VA COVID-19 procurements : pandemic underscores urgent need to modernize supply chain : report to congressional committees.
Published: (2021)

Wearable and implantable medical devices : applications and challenges /
Published: (2020)

Medical devices & equipment : standards, design, failures & safety : medical subject analysis and research index with bibliography /
by: Donovan, Chester D. (Chester Donne)
Published: (1984)

Medical device epidemiology and surveillance /
Published: (2007)

Medical product liability : a comprehensive guide and sourcebook /
Published: (1981)

Medical devices : are current regulations doing enough for patients? : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Eleventh Congress, first session, June 18, 2009.
Published: (2012)

Medical equipment and supplies : purchases and rentals, expenditures, and sources of payment /
by: Hagan, Michael
Published: (1982)

Reliable design of medical devices /
by: Fries, Richard C.
Published: (2006)

Managing the risks from medical product use : creating a risk management framework : report to the FDA Commissioner from the Task Force on Risk Management.
Published: (1999)

FDA's clearance of medical devices through the 510(k) process.
Published: (2013)

Economic organization in medical equipment and supply /
by: Peterson, Rodney D.
Published: (1973)

Approval of medical devices.
Published: (2014)

Federal policies and the medical devices industry.
Published: (1984)

Federal policies and the medical devices industry.
Published: (1984)

Medical device establishment registration : information and instructions.
Published: (1987)

Medical devices : application of risk management to medical devices = Dispositifs médicaux : application de la gestion des risques aux dispositifs médicaux.
Published: (2019)

Usability testing of medical devices /
by: Wiklund, Michael E.
Published: (2011)

Medical device regulation : FDA-CDRH manufacturing, policies and regulation handbook /
by: Wreh, Elijah
Published: (2023)

Medical device regulation in the United States and the European community /
by: Reyes-Akinbileje, Bernice
Published: (1992)

Medical devices and the FDA : regulation, user fees and tort claims /
Published: (2013)

Medical instrumentation : application and design /
Published: (1998)

Medical devices : technological innovation and patient/provider perspectives : hearing before the Subcommittee on Health and Environment of the Committee on Commerce, House of Representatives, One Hundred Fifth Congress, first session, May 30, 1997.
Published: (1997)

COVID-19 medical countermeasures : intellectual property and affordability /
by: Hickey, Kevin J.
Published: (2020)

Medical devices : guidance on the application of ISO 14971 = Dispositifs médicaux : recommandations relatives à l'application de l'ISO 14971.
Published: (2020)

Medical devices and the public's health : the FDA 510(k) clearance process at 35 years /
Published: (2011)

Medical devices--measurements, quality assurance, and standards /
Published: (1983)

The future of medical device regulation : innovation and protection /
Published: (2022)