Health : drugs and medical devices : agreement between the United States of America and China, signed at Beijing, December 11, 2007. by United States, United States, China

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Consejos sobre los medicamentos y los dispositivos al cuidar de otros.

Subjects: “…Medical instruments and apparatus.…”
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Caring for others : tips for medicines and devices.

Subjects: “…Medical instruments and apparatus.…”
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USAMRMC products portfolio /

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The law and regulation of medicines and medical devices / by Feldschreiber, Peter, Oxford Scholarship Online

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Guidance for industry "help-seeking" and other disease awareness communications by or on behalf of drug and device firms. by Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.), Center for Devices and Radiological Health (U.S.)

Subjects: “…Advertising Medical instruments and apparatus United States.…”
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Food and Drug Administration FDA faces challenges meeting its growing medical product responsibilities and should develop complete estimates of its resource needs : report to congr... by United States. Government Accountability Office

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Guidance for industry presenting risk information in prescription drug and medical device promotion. by Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.), Center for Veterinary Medicine (U.S.), Center for Devices and Radiological Health (U.S.)

Subjects: “…Advertising Medical instruments and apparatus.…”
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Journal of medical marketing. by Sage Journals Online

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21st century cures : modernizing clinical trials : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Thirteen... by United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

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FDA user fees and the regulation of drugs, biologics, and devices : comparative analysis of S. 3187 and H.R. 5651 / by Thaul, Susan

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Medical product innovation and regulation : benefits vs. risks / by Johnson, Judith A. (Judith Ann), 1957-

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Medical product innovation and regulation : benefits and risks / by Dabrowska, Agata, Sarata, Amanda K., Green, Victoria R.

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Medical product regulation : drugs, biologics, and devices / by Dabrowska, Agata, Green, Victoria R.

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Should FDA drug and medical device regulation bar state liability claims? hearing before the Committee on Oversight and Government Reform, House of Representatives, One Hundred Ten... by United States. Congress. House. Committee on Oversight and Government Reform

Subjects: “…Products liability Medical instruments and apparatus United States.…”
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Guidance for industry container and closure system integrity testing in lieu of sterility testing as a component of the stability protocol for sterile products. by Center for Biologics Evaluation and Research (U.S.), Center for Drug Evaluation and Research (U.S.), Center for Devices and Radiological Health (U.S.), Center for Veterinary Medicine (U.S.)

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Guidance for industry preparation of IDEs and INDs for products intended to repair or replace knee cartilage. by Center for Biologics Evaluation and Research (U.S.)

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Food and Drug Administration Reform Act of 2012 report (to accompany H.R. 5651) (including cost estimate of the Congressional Budget Office). by United States. Congress. House. Committee on Energy and Commerce

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Food and Drug Administration Amendments Act of 2007 : report together with additional views (to accompany H.R. 2900) (including cost estimate of the Congressional Budget Office). by United States. Congress. House. Committee on Energy and Commerce

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Guidance for industry patient-reported outcome measures, use in medical product development to support labeling claims. by Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.), Center for Devices and Radiological Health (U.S.)

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