Current Status Bill Number:1185 Type of Legislation:Concurrent Resolution CR Introducing Body:Senate Introduced Date:19960227 Primary Sponsor:Russell All Sponsors:Russell and Giese Drafted Document Number:bbm\10606jm.96 Date Bill Passed both Bodies:19960404 Subject:New drugs, biological products, medical devices
Body Date Action Description Com Leg Involved ______ ________ _______________________________________ _______ ____________ Senate 19960404 Received from House House 19960403 Adopted, returned to Senate with concurrence House 19960328 Committee report: Favorable 24 HIMR House 19960326 Introduced, referred to Committee 24 HIMR Senate 19960321 Adopted, sent to House Senate 19960314 Committee report: Favorable 13 SMA Senate 19960227 Introduced, referred to Committee 13 SMAView additional legislative information at the LPITS web site.
COMMITTEE REPORT
March 28, 1996
S. 1185
S. Printed 3/28/96--H.
Read the first time March 26, 1996.
To whom was referred a Concurrent Resolution (S. 1185), memorializing Congress to amend the federal Food, Drug, and Cosmetic Act, etc., respectfully
That they have duly and carefully considered the same, and recommend that the same do pass:
RICHARD M. QUINN, JR., for Committee.
MEMORIALIZING CONGRESS TO AMEND THE FEDERAL FOOD, DRUG, AND COSMETIC ACT AND THE PUBLIC HEALTH SERVICE ACT TO FACILITATE THE DEVELOPMENT AND APPROVAL OF NEW DRUGS, BIOLOGICAL PRODUCTS, AND MEDICAL DEVICES.
Whereas, improving patient access to quality health care is a paramount national goal; and
Whereas, the key to improved health care, especially for persons with serious, unmet medical needs, is the rapid approval of safe and effective new drugs, biological products, and medical devices; and
Whereas, minimizing the delay between discovery and eventual approval of a new drug, biological product, or medical device derived from research conducted by innovative pharmaceutical and biotechnology companies could improve the lives of millions of Americans; and
Whereas, current limitations on the dissemination of information about pharmaceutical products reduce the availability of information to physicians, other health care professionals, and patients and unfairly limit the right of free speech guaranteed by the First Amendment to the United States Constitution; and
Whereas, current rules and practices governing the review of new drugs, biological products, and medical devices by the United States Food and Drug Administration can delay approvals and are unnecessarily expensive. Now, therefore,
Be it resolved by the Senate, the House of Representatives concurring:
That the General Assembly of the State of South Carolina, by this resolution, memorializes Congress to amend the federal Food, Drug, and Cosmetic Act and the Public Health Service Act to facilitate the development and approval of new drugs, biological products, and medical devices.
Be it further resolved that copies of this resolution be forwarded to each member of the South Carolina Congressional Delegation, the President of the United States Senate, and the Speaker of the United States House of Representatives, all at Washington, D.C.