| Literature DB >> 16886819 |
Abstract
Medical device manufacturers do not always properly control the development of new or modified promotional labelling and advertising materials. This lack of control can lead to unexpected regulatory problems. This article discusses United States requirements for these materials and the type of controls that companies should exercise.Mesh:
Year: 2006 PMID: 16886819
Source DB: PubMed Journal: Med Device Technol ISSN: 1048-6690