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Regulatory affairs for biomaterials and medical devices
All biomaterials and medical devices are subject to a long list of regulatory practises and policies which must be adhered to in order to receive clearance. This book provides readers with information on the systems in place in the USA and the rest of the world. Chapters focus on a series of procedu...
| Autores principales: | , , |
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| Lenguaje: | eng |
| Publicado: |
Elsevier Science
2015
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| Materias: | |
| Acceso en línea: | http://cds.cern.ch/record/2124157 |