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  • Compliance for software validation in 21 CFR Part 11 - 2017

    Compliance for software validation in 21 CFR Part 11 - 2017

    Training and Teaching Zurich (Opfikon) February 16, 2017 1695.00 Dollar US$

    Overview: Since July 2013, Regulation (EC) No 1223/2009 on Cosmetic Products of the EU has been fully implemented and represents a modern regulatory framework grounded on state of the art of cosmetic science and product technology. It is structured i...

  • 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...

  • Drug Master Files and Quality Agreement Training Seminar 2018

    Drug Master Files and Quality Agreement Training Seminar 2018

    Drug Development Philadelphia (PA,PA) March 6, 2018 1495.00 Dollar US$

    Overview: This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, there have been several misunderstandings be...

  • Data Integrity, 21 CFR 11 & Annex 11 Implementation 2017

    Data Integrity, 21 CFR 11 & Annex 11 Implementation 2017

    Training and Teaching SFO, CA (SFO, CA) October 23, 2017 1495.00 Dollar US$

    Course "Data Integrity, 21 CFR 11 & Annex 11 Implementation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: The Problem: We have all heard of Data Integri...

  • Regulatory Requirements and Principles for Cleaning Validation 2017

    Regulatory Requirements and Principles for Cleaning Validation 2017

    Training and Teaching San Diego, CA ( San Diego, CA) October 23, 2017 1495.00 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 2day course will cover practical g...

  • Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)

    Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)

    Training and Teaching Philadelphia, PA (Philadelphia, PA) March 24, 2017 1495.00 Dollar US$

    This workshop style training course is supported by comprehensive knowledge of U.S. FDA laws and regulations and 30 year of extensive experience working within in the U.S. FDA regulated industries. In these 2 days, the following essential topics will...

  • Audit Like the FDA Audit Like the FDA 2017 before 30 April 50% Discount for its All Seminars

    Audit Like the FDA Audit Like the FDA 2017 before 30 April 50% Discount for its All Seminars

    Training and Teaching Boston, MA (Boston, MA) March 24, 2017 1495.00 Dollar US$

    This 2 day seminar will explore how to create and implement an efficient and effective internal audit program. Internal Audit is a required part of an effective quality system. More importantly, it is an incredibly powerful tool to identify areas of ...

  • HIPAA Security & Privacy Officials Training 2017

    HIPAA Security & Privacy Officials Training 2017

    Training and Teaching Baltimore, MD (The DoubleTree Baltimore-BWI Airport) February 24, 2017 1495.00 Dollar US$

    Overview: Being the HIPAA Security and Privacy Official involves not only ensuring you know the appropriate patient rights and controls on your uses and disclosures of protected health information, but you also have the proper policies and procedures...

  • Clinical Data Management Seminar 2018

    Clinical Data Management Seminar 2018

    Clinical New Orleans (lousiana) July 5, 2018 1295.00 Dollar US$

    When new drugs or devices are tested in humans, the data generated by, and related to, these trials is known as clinical data. This data represents a huge investment by the biopharmaceutical or device company and is one of its greatest assets. It is ...