ResearchBib Share Your Research, Maximize Your Social Impacts
Sign for Notice Everyday Sign up >> Login

Searching Call For Papers

Category Year
Country
Keywords From

Searching Results

  1. ISO 14971 Risk Management Training-IEC 62304 Risk Management
    Deadline: 2018-03-26 Event Date: 2018-03-27 - 2018-03-28
    Venue: Zurich, Switzerland, Swaziland
  2. 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
  3. Medical Device Supplier Management Training | Switzerland
    Deadline: 2018-03-11 Event Date: 2018-03-12 - 2018-03-13
    Venue: Zurich, Switzerland, Swaziland
  4. Medical Device Registration and Listing | Japan, Australia
    Deadline: 2018-02-05 Event Date: 2018-02-07 - 2018-02-08
    Venue: Zurich, Switzerland, Swaziland
  5. 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
  6. 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
  7. 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
  8. 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
  9. Data Integrity FDA/EU Requirements and Implementation 2017
    Deadline: 2017-09-25 Event Date: 2017-09-27 - 2017-09-28
    Venue: Zurich, Switzerland, Swaziland
  10. European Regulatory Procedures 2017
    Deadline: 2017-08-22 Event Date: 2017-08-28 - 2017-08-29
    Venue: Zurich, Switzerland, Swaziland