2011 Qserve Training Course Schedule
CE Marking, FDA 510(k) Compliance, CMDR,
ISO 13485, FDA/QSR, CMDCAS,
Auditing, Risk management ISO 14971, Design and Development
* courses are organized by and in conjunction with 
in The Netherlands
| Location | Course | Language | Duration | Date | Price | |
|---|---|---|---|---|---|---|
| Antwerpen* | Introduction ISO 13485 | NL/ENG | 1 day | Sep. 14 | ||
| Antwerpen* | Introduction ISO 13485 | NL/ENG | 1 day | Sep. 14 | Contact us |
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| Antwerpen* | Introduction ISO 13485 | NL/ENG | 1 day | Sep. 14 | Contact us |
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| Antwerpen* | Implementation ISO 13485 | NL/ENG | 2 days | Oct. 5/6 | Contact us |
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| Antwerpen* | Internal auditor ISO 13485 | NL/ENG | 2 days | Sep. 21/22 | Contact us |
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| Antwerpen* | Lead auditor ISO 13485 | NL/ENG | 5 days | Dec. 12/16 | Contact us |
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| Amsterdam* | Risk Management ISO 14971 | NL/ENG | 1 day | Oct. 4 | Contact us |
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| Antwerpen* | Introduction CE Marking | NL/ENG | 1 day | May 31 | Contact us |
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| Arnhem* | Introduction CE Marking | NL/ENG | 1 day | Nov. 15 | Contact us |
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| Antwerpen* | Medical Devices CE Marking | NL/ENG | 3 days | Nov. 8/10 | Contact us |
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| Amsterdam* | Diagnostica richtlijn | NL/ENG | 1 day | Oct. 13 | Contact us |
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| Arnhem* | Post Market Surveillance and Vigilance | NL/ENG | 1 day | Sep. 27 | Contact us |
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| Amsterdam* | Device-Drug Combinaties | NL/ENG | 1 day | Jun. 29, Sep. 8 | Contact us |
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| Amsterdam* | Proces Validatie Medische Hulpmiddelen | NL/ENG | 1 day | Oct. 13 | Contact us |
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| Amsterdam* | Toepassing In Vitro Diagnostica (IVD) Richtlijn | NL/ENG | 3 days | Nov. 1/3 | Contact us |
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