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  • Medical Device Supplier Management Training | Switzerland

    Medical Device Supplier Management Training | Switzerland

    Training and Teaching Zurich, Switzerland ( Zurich, Switzerland) January 19, 2018 1695.00 Dollar US$

    Overview: Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your...

  • Regulatory Requirements Cleaning Validation | FDA Guidelines 2018

    Regulatory Requirements Cleaning Validation | FDA Guidelines 2018

    Training and Teaching Zurich ( Zurich, Switzerland) January 19, 2018 1695.00 Dollar US$

    Course "Regulatory Requirements and Principles for Cleaning Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This 2 day course will cover practical ...

  • What is Process Validation Report | 21CFR11 Compliance Checklist 2018

    What is Process Validation Report | 21CFR11 Compliance Checklist 2018

    Training and Teaching Germany (Germany) November 9, 2017 1695.00 Dollar US$

    Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also kn...

  • Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

    Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

    Drug Development Zurich, Switzerland ( Zurich, Switzerland) November 9, 2017 1695.00 Dollar US$

    Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also kn...

  • 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 ...

  • 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...

  • 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...

  • 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...

  • 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...

  • The EU General Data Protection Regulation (GDPR) 2017

    The EU General Data Protection Regulation (GDPR) 2017

    Training and Teaching London, UK (London, UK) July 14, 2017 1695.00 Dollar US$

    Course "The EU General Data Protection Regulation (GDPR)" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: On 25th May 2018 the EU-GDPR becomes effective, this ...

  • European Regulatory Procedures 2017

    European Regulatory Procedures 2017

    Training and Teaching Zurich, Switzerland (Hilton Zurich Airport) June 15, 2017 1695.00 Dollar US$

    Course "European Regulatory Procedures - Comprehensive Overview of EMA and National Requirements and other Agencies" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Over...

  • Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements 2017

    Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements 2017

    Training and Teaching INTERCONTINENTAL HONG KONG (Hong Kong) April 24, 2017 1695.00 Dollar US$

    Course "Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: • Defin...