Practical information about the complexities of biomedical technology and regulation, and their implications for manufacturers and marketers of health care devices. Written primarily for those in the industry concerned about staying competitive in light of complex and fluctuating regulatory approachConsequently, labeling instructions should be as short and simple as possible. In drafting ... Consequently, particularly for Section 510(k) devices, poorly written instruction manuals tend to breed additional poorly written instruction manuals.
|Title||:||The Medical Device Industry|
|Author||:||Norman F. Estrin|
|Publisher||:||CRC Press - 1990-08-31|