Quality Control, Safety & Security

Listings
  • 21 CFR Part 11 compliance for software validation and SaaS/Cloud 2017

    21 CFR Part 11 compliance for software validation and SaaS/Cloud 2017

    Quality Control, Safety & Security Zurich, Switzerland (Hilton Zurich Airport) August 23, 2017 1695.00 Dollar US$

    Course "21 CFR Part 11 compliance for software validation and SaaS/Cloud" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: • This interactive two-day course exp...

  • Regulatory Filing Requirements and Compliance Processes for Medical Devices 2017

    Regulatory Filing Requirements and Compliance Processes for Medical Devices 2017

    Quality Control, Safety & Security Zurich, Switzerland (Hilton Zurich Airport) August 23, 2017 1695.00 Dollar US$

    Course "Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: • Japan's classifi...

  • Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices 2017

    Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices 2017

    Quality Control, Safety & Security Singapore (Mandarin Orchard Singapore) August 23, 2017 1695.00 Dollar US$

    Course "Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: • Japan's classifi...

  • Validation, Verification and Transfer of Analytical Methods from FDA/EMA, USP and ICH 2017

    Validation, Verification and Transfer of Analytical Methods from FDA/EMA, USP and ICH 2017

    Quality Control, Safety & Security Zurich, Switzerland (Mövenpick Hotel Zurich-Airport) August 23, 2017 1695.00 Dollar US$

    Course "Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon...

  • The EU Clinical Trial Regulation + EU Filings & Registrations 2017

    The EU Clinical Trial Regulation + EU Filings & Registrations 2017

    Quality Control, Safety & Security Zurich, Switzerland (Hilton Zurich Airport) September 21, 2017 1695.00 Dollar US$

    Course "The EU Clinical Trial Regulation + EU Filings & Registrations" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This course covers the requirements ...

  • Quality by Design using Design of Experiments (QbD) 2017

    Quality by Design using Design of Experiments (QbD) 2017

    Quality Control, Safety & Security Singapore (Singapore) April 24, 2017 1695.00 Dollar US$

    Course "Quality by Design using Design of Experiments (QbD)" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This seminar focuses on how to establish a systema...

  • GMP requirements for quality control and contract laboratories 2017

    GMP requirements for quality control and contract laboratories 2017

    Quality Control, Safety & Security Singapore (Singapore) October 26, 2016 1895.00 Dollar US$

    Overview: Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further check. That's the reason...

  • GMP requirements for quality control and contract laboratories 2017

    GMP requirements for quality control and contract laboratories 2017

    Quality Control, Safety & Security Singapore (Singapore) October 26, 2016 1895.00 Dollar US$

    Overview: Quality control and related contract laboratories are considered at high risk because after testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further check. That's the reason...