1.
Med Device Technol
; 8(2): 38-44, 46, 48, 1997 Mar.
Article
in English
| MEDLINE
| ID: mdl-10166366
ABSTRACT
The medical device industry in the United States is facing a number of challenges, for example, work on Food and Drug Administration reform and a global move towards European-style regulation and harmonization. This article examines those challenges and their effect on the industry and on patients.
Subject(s)
Equipment and Supplies/standards , Industry/legislation & jurisprudence , United States Food and Drug Administration/legislation & jurisprudence , Device Approval , Europe , United States
2.
Health Syst Rev
; 24(3): 34-43, 1991.
Article
in English
| MEDLINE
| ID: mdl-10110624
ABSTRACT
A panel of experts responded to the Health Care Financing Administration's proposed capital reimbursement regulations at the recent Annual Conference of the Federation of American Health Systems in Orlando, Florida. What follows are edited versions of some of the panelists--but not all--concerning the issue and HCFA's position.
