1 Medical Device Regulatory Compliance Consultants - Schedule

 
 

2010 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 conjuction with  in The Netherlands

Contact us, click here

Location Course Language Duration Date Price
Amsterdam* Introduction to ISO 13485 NL/ENG 1 day June 01 contact us.
Eindhoven* Introduction to ISO 13485 NL/ENG 1 day June 08 contact us
Amsterdam* Introduction to ISO 13485 NL/ENG 1 day Oct. 13 contact us
Amsterdam* Implementing to: ISO 13485 NL/ENG 2 days Sept.08/09 contact us
Amsterdam * Internal auditor ISO 13485 NL/ENG two days Sept.22/23 contact us
Amsterdam * Lead auditor: ISO 13485 NL/ENG 5 days Nov.01/05 contact us
Amsterdam* Introduction to CE Marking NL/ENG 1 day Sept. 15 contact us
Amsterdam* Medical Devices CE Marking NL/ENG 3 days Oct.05/07 contact us
Amsterdam* Medical Device Risk Management NL/ENG 1 day June 15 contact us
Amsterdam* Post Market Surveillance and Vigilance NL/ENG 1 day June 22 contact us
In company Medical Device Risk Management NL/ENG TBD TBD contact us
Eindhoven* Post Market Surveillance and Vigilance NL/ENG 1 day June 29 contact us
Amsterdam* Post Market Surveillance and Vigilance NL/ENG 1 day Oct. 20 contact us
Amsterdam FDA regulations ENG 1 day TBD contact us
Amsterdam* Drug and Device combination Products ENG 1 day July contact us
Amsterdam Technical Documentation STED NL/ENG 05, day TBD contact us
Boston FDA regulations ENG 1 day TBD contact us
Amsterdam Veiligheidsmanagement medische technologie in ziekenhuizen NL 1 day Sept. 15 contact us
Amsterdam Kwaliteitsborging medische technologie in ziekenhuizen NL 1 day Oct. 5 contacts us
Amsterdam Kwaliteit en veiligheid medische technologie in ziekenhuizen NL 1 day Oct.20 contact us
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