Pertains to the clinical investigation in human subjects of those medical devices whose clinical performance needs assessment. Specifies the requirements for conducting the clinical investigation and documentation. Provides the framework for systematic written procedures for the organization, design, implementation and data collection.
Текущий статус : WithdrawnДата публикации : 1996-02
Версия : 1Число страниц : 12
Технический комитет:Biological and clinical evaluation of medical devices