Hearing on "Regulatory Reform Series #5 - FDA Medical Device Regulation: Impact on American Patients, Innovation, and Jobs"

Format:

Book

Government document

Author/Creator:

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations

Language:

English

Subjects (All):

Medical laws and legislation.

Medical supplies.

Physical Description:

1 online resource

Contained In:

ProQuest U.S. Congressional Research Digital Collection

Place of Publication:

[United States] [publisher not identified] 2011

Summary:

Memorandum, prepared by Subcom on Oversight and Investigations Republican majority staff in light of upcoming July 20, 2011, Subcom hearing, examining FDA medical device classification and review processes

Notes:

Print

Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection (last viewed Feb. 2013). Reuse except for individual research requires license from ProQuest, LLC

Vendor supplied data

Other Format:

Microfiche version United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations. Hearing on "Regulatory Reform Series #5 - FDA Medical Device Regulation: Impact on American Patients, Innovation, and Jobs". 2011 H362-247

Publisher Number:

CMP-2011-HEC-0240

Access Restriction:

Restricted for use by site license