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  • 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...

  • ISO 14971 Risk Management Training-IEC 62304 Risk Management

    ISO 14971 Risk Management Training-IEC 62304 Risk Management

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

    Course "Applying ISO14971 and IEC62304 - A guide to practical Risk Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Gaps, incorrect or incomplete im...

  • Supplier Management Solutions | Medical Device Manufacturers

    Supplier Management Solutions | Medical Device Manufacturers

    Training and Teaching Frankfurt, Germany ( Frankfurt, Germany) 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...

  • 21 CFR Part 11 Compliance Checklist- FDA Software Validation

    21 CFR Part 11 Compliance Checklist- FDA Software Validation

    Training and Teaching Zurich, Switzerland ( Zurich, Switzerland) January 19, 2018 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...

  • 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...