| 000 | 01247cam a2200301Ii 4500 | ||
|---|---|---|---|
| 001 | 9780429091469 | ||
| 008 | 180331t20162016fluad ob 001 0 eng d | ||
| 020 |
_a9780429091469 _q(e-book : PDF) |
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| 020 |
_z9789814669108 _q(hardback) |
||
| 024 | 7 |
_a10.1201/b18817 _2doi |
|
| 035 | _a(OCoLC)919252277 | ||
| 040 |
_aFlBoTFG _cFlBoTFG _erda |
||
| 050 | 4 |
_aK3611.M45 _bT44 2016 |
|
| 082 | 0 | 4 |
_a344.041 _bT377 |
| 100 | 1 |
_aTheisz, Val, _eauthor. _911258 |
|
| 245 | 1 | 0 |
_aMedical device regulatory practices : _ban international perspective / _cVal Theisz. |
| 264 | 1 |
_aBoca Raton : _bCRC Press, _c[2016] |
|
| 264 | 4 | _c©2016 | |
| 300 | _a1 online resource | ||
| 336 |
_atext _2rdacontent |
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| 337 |
_acomputer _2rdamedia |
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| 338 |
_aonline resource _2rdacarrier |
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| 505 | 0 | _a1. Overview of the international regulatory framework for medical devices -- 2. Safety and effectiveness -- 3. Technical documentation -- 4. Pre-market phase -- 5. Regulatory submissions, approvals and registrations -- 6. Post-market phase. | |
| 650 | 0 |
_aMedical instruments and apparatus _xSafety regulations. _911259 |
|
| 776 | 0 | 8 |
_iPrint version: _z9789814669108 |
| 856 | 4 | 0 |
_uhttps://www.taylorfrancis.com/books/9789814669115 _zClick here to view. |
| 942 | _cEBK | ||
| 999 |
_c69922 _d69922 |
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