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1. 21 CFR Part 11 Compliance Checklist- FDA Software Validation
   Deadline: 2018-03-13 Event Date: 2018-03-14 - 2018-03-15
   Venue: Zurich, Switzerland, Swaziland
2. Medical Device Supplier Management Training | Switzerland
   Deadline: 2018-03-11 Event Date: 2018-03-12 - 2018-03-13
   Venue: Zurich, Switzerland, Swaziland
3. Medical Device Registration and Listing | Japan, Australia
   Deadline: 2018-02-05 Event Date: 2018-02-07 - 2018-02-08
   Venue: Zurich, Switzerland, Swaziland
4. The EU Clinical Trial Regulation + EU Filings & Registrations 2017
   Deadline: 2017-11-01 Event Date: 2017-11-02 - 2017-11-03
   Venue: Zurich, Switzerland, Swaziland
5. Validation, Verification and Transfer of Analytical Methods from FDA/EMA, USP and ICH 2017
   Deadline: 2017-10-23 Event Date: 2017-10-25 - 2017-10-26
   Venue: Zurich, Switzerland, Swaziland
6. Regulatory Filing Requirements and Compliance Processes for Medical Devices 2017
   Deadline: 2017-10-10 Event Date: 2017-12-12 - 2017-12-13
   Venue: Zurich, Switzerland, Swaziland
7. 21 CFR Part 11 compliance for software validation and SaaS/Cloud 2017
   Deadline: 2017-10-10 Event Date: 2017-12-12 - 2017-12-13
   Venue: Zurich, Switzerland, Swaziland
8. Data Integrity FDA/EU Requirements and Implementation 2017
   Deadline: 2017-09-25 Event Date: 2017-09-27 - 2017-09-28
   Venue: Zurich, Switzerland, Swaziland
9. European Regulatory Procedures 2017
   Deadline: 2017-08-22 Event Date: 2017-08-28 - 2017-08-29
   Venue: Zurich, Switzerland, Swaziland
10. Validation and Part 11 Compliance of Computer Systems and Data 2017
    Deadline: 2017-07-08 Event Date: 2017-07-11 - 2017-07-12
    Venue: Hilton Zurich Airport, Swaziland

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