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  • Supplier Management Conference for Medical Device Manufacturing in HONG KONG

    Supplier Management Conference for Medical Device Manufacturing in HONG KONG

    Training and Teaching HONG KONG (INTERCONTINENTAL HONG KONG) January 27, 2017 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...

  • Risk Management Seminar for Applying ISO14971 and IEC62304

    Risk Management Seminar for Applying ISO14971 and IEC62304

    Training and Teaching Zurich (Zurich) January 25, 2017 1695.00 Dollar US$

    Overview: Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the devel...

  • Supplier Management Conference for Medical Device Manufacturing in Switzerland

    Supplier Management Conference for Medical Device Manufacturing in Switzerland

    Training and Teaching Zurich (Zurich) January 25, 2017 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...

  • Validation, Verification and Transfer of Analytical Methods 2017

    Validation, Verification and Transfer of Analytical Methods 2017

    Training and Teaching Zurich, Switzerland (United States ) January 10, 2017 1695.00 Dollar US$

    Overview: Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method an...

  • Tougher Import Rules for FDA Imports in 2018

    Tougher Import Rules for FDA Imports in 2018

    Data Management Raleigh (North Carolina) October 25, 2018 1495.00 Dollar US$

    Description: FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and adherence to government procedures. Firms that fail to understand and properly e...

  • Excel Spreadsheet Validation 2018 Tools and Techniques

    Excel Spreadsheet Validation 2018 Tools and Techniques

    Clinical Salt Lake City (Utah) October 25, 2018 1495.00 Dollar US$

    Description: Spreadsheets such as Excel, are available for creating a wide range of end user applications, including widespread use in the laboratory, creating customized statistical analyses, the creation of local databases, data mining, and multiva...

  • 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...

  • HIPAA Compliance - Clear, Complete, Step-by-Step

    HIPAA Compliance - Clear, Complete, Step-by-Step

    Training and Teaching San Diego (California) October 25, 2018 1495.00 Dollar US$

    Description: Organizations of all types and sizes continue to struggle needlessly with HIPAA Compliance. For example, HIPAA Risk Analysis – Risk Management is the basis of the HIPAA Compliance Program of every Covered Entity and Business Associate. B...

  • Quality by Design - Essential Techniques for Medical Devices

    Quality by Design - Essential Techniques for Medical Devices

    Chemical Methods San Diego (California) October 25, 2018 1495.00 Dollar US$

    Description: Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet, Design Controls are still one of the most frequent areas for 483 and Warning Letter ob...

  • OSHA Recordkeeping and Surviving an OSHA Audit

    OSHA Recordkeeping and Surviving an OSHA Audit

    Clinical New Orleans (Louisiana) October 25, 2018 1495.00 Dollar US$

    Description: The Occupational Safety and Health Administration (OSHA) has jurisdiction to protect the workers of America and its territories from harmful working conditions. They are a department under the US Department of Labor and was given the leg...

  • Applied Statistics for Scientists and Engineers seminar at Boston

    Applied Statistics for Scientists and Engineers seminar at Boston

    Training and Teaching Boston (Massachusetts) October 25, 2018 1495.00 Dollar US$

    Description: Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting validation criteria and specifications, performing measu...

  • Japan Regulatory Compliance Requirements for Life Science Products

    Japan Regulatory Compliance Requirements for Life Science Products

    Drug Development Seattle (Washington) September 5, 2018 1495.00 Dollar US$

    Course "Japan Regulatory Compliance Requirements for Life Science Products" 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 seminar covers the detai...