Improving product introduction through effective design reviews.

Publisher: Published by Hanley & Belfus for the Association Country of Publication: United States NLM ID: 8905560 Publication Model: Print Cited Medium: Print ISSN: 0899-8205 (Print) Linking ISSN: 08998205 NLM ISO Abbreviation: Biomed Instrum Technol Subsets: MEDLINE

Original Publication: [Philadelphia, PA : Published by Hanley & Belfus for the Association, c1989-

Biotechnology/*organization & administration ; Equipment Design/*methods ; Equipment Design/*standards ; Equipment and Supplies/*standards ; Technology Assessment, Biomedical/*organization & administration; Biotechnology/instrumentation ; Biotechnology/methods ; Decision Making, Organizational ; Marketing/methods ; Quality Control ; Technology Assessment, Biomedical/methods ; United States

The design review process is a part of the manufacturer's due diligence in developing a safe and effective product. Design review provides early and on-going independent feedback to developers. By adopting a proactive review process, design improvements can be pursued at an optimum time in the product development effort, i.e., when it will cost less to implement changes and when these changes may have the greatest impact. Effective implementation of the design review requirement will lead to better medical products and improved product introduction results.

Date Created: 20030408 Date Completed: 20030701 Latest Revision: 20220723

20240829

10.2345/0899-8205(2003)37[131:IPITED]2.0.CO;2

12677754