Work

FDA Regulation of Medical Devices

Year: 2012

Type: report

Abstract: This report provides a description of FDA's medical device review process divided into two parts: pre market requirements and post market requirements. Appendix A provides a brief history of laws governing medical device regulation and Appendix B provides a table of acronyms used in the report.

Source: University of North Texas Digital Library (University of North Texas)

Author: Judith A. Johnson

Language: English

Topic: Healthcare Regulation

Subfield: Public Health, Environmental and Occupational Health

Field: Medicine

Domain: Health Sciences

Open Access status: green

OpenAlex ID: W2522780295

Cites:

Cited by: 34

Related to: 10