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...

  • Introduction to Adaptive Design for Clinical Trials

    Introduction to Adaptive Design for Clinical Trials

    Quality Control, Safety & Security Philadelphia (Pennsylvania) October 25, 2018 1495.00 Dollar US$

    Description: This 2-day seminar includes an overview of Adaptive Design, and an emphasis in group sequential design, sample size re-estimation, and Phase II/III Adaptive Seamless Designs. The role of statistics in clinical trials incorporates the too...

  • FDA's Software Monsters Cybersecurity, Interoperability, Mobile Apps 2017

    FDA's Software Monsters Cybersecurity, Interoperability, Mobile Apps 2017

    Quality Control, Safety & Security SFO, CA (SFO, CA) July 14, 2017 1295.00 Dollar US$

    Course "FDA's Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Software's level of...

  • Validation and Troubleshooting of Pharmaceutical Water Systems 2017

    Validation and Troubleshooting of Pharmaceutical Water Systems 2017

    Quality Control, Safety & Security Sydney, Australia (Sydney, Australia) July 14, 2017 1295.00 Dollar US$

    Course "The A to Z's of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Ov...

  • Supplier Management in FDA- and ISO-regulated Industry 2017

    Supplier Management in FDA- and ISO-regulated Industry 2017

    Quality Control, Safety & Security San Diego, CA (San Diego, CA) July 14, 2017 1295.00 Dollar US$

    Course "Supplier Management in FDA- and ISO-regulated Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Supplier qualification and assessment is requir...

  • FDA FSMA Rules & Planning Valid Preventive Food Safety Controls 2017

    FDA FSMA Rules & Planning Valid Preventive Food Safety Controls 2017

    Quality Control, Safety & Security San Diego, CA ( San Diego, CA) July 14, 2017 1295.00 Dollar US$

    Course "Preparing to Comply with the New FDA FSMA Rules: Planning Valid Preventive Food Safety Controls" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Upon c...

  • Applied Statistics for FDA Process Validation 2017

    Applied Statistics for FDA Process Validation 2017

    Quality Control, Safety & Security Baltimore, MD (Baltimore, MD) July 14, 2017 1295.00 Dollar US$

    Course "Applied Statistics for FDA Process Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: In Guidance for Industry Process Validation: General Pri...