Pharmacology - Drug Development

Listings
  • Combination Products

    Combination Products

    Pharmacology - Drug Development Salt Lake City (Utah) September 5, 2018 Check with publisher

    Course "Combination Products" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Description: This seminar provides Professionals working in this area with: • A thorough un...

  • Effective Complaint Handling, Medical Device Reporting and Recalls

    Effective Complaint Handling, Medical Device Reporting and Recalls

    Pharmacology - Drug Development Baltimore (Maryland) December 6, 2019 Check with publisher

    An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corr...

  • Strategies for Improving Effectiveness and Efficiency of your Quality Management System

    Strategies for Improving Effectiveness and Efficiency of your Quality Management System

    Pharmacology - Drug Development Salt Lake City (Utah) September 5, 2018 Check with publisher

    Course "Strategies for Improving Effectiveness and Efficiency of your Quality Management System" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Description: This two-da...

  • FDA Scrutiny of Promotion and Advertising Practices

    FDA Scrutiny of Promotion and Advertising Practices

    Pharmacology - Drug Development San Francisco (California) September 5, 2018 Check with publisher

    Course "FDA Scrutiny of Promotion and Advertising Practices" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Description: If you go "off label" with advertising and prom...

  • Validation and 21 CFR Part 11 Compliance of Computer Systems

    Validation and 21 CFR Part 11 Compliance of Computer Systems

    Pharmacology - Drug Development Philadelphia (Pennsylvania) September 5, 2018 Check with publisher

    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. Description: The Problem We have all heard of Compu...

  • US, EU and Japan GMP Requirements

    US, EU and Japan GMP Requirements

    Pharmacology - Drug Development Minnesota (Minneapolis) September 5, 2018 Check with publisher

    Course "US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus " has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Descri...

  • Wnt1 peptide

    Wnt1 peptide

    Pharmacology - Drug Development Shirley (New York) February 22, 2019 Check with publisher

    The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during em...

  • ZSCAN4 peptide

    ZSCAN4 peptide

    Pharmacology - Drug Development Shirley (New York) February 22, 2019 Check with publisher

    The ZSCAN4 gene encodes a protein involved in telomere maintenance and with a key role in the critical feature of mouse embryonic stem (ES) cells, namely, defying cellular senescence and maintaining normal karyotype for many cell divisions in culture...

  • A Risk Based Approach to IT Infrastructure Seminar 2018

    A Risk Based Approach to IT Infrastructure Seminar 2018

    Pharmacology - Drug Development Minnesota (Miss) April 2, 2018 Check with publisher

    Course "A Risk Based Approach To IT Infrastructure & Cloud Qualification, Compliance & Control" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: GxP Reg...

  • Process Validation General Principle and Practices - Philadelphia 2018

    Process Validation General Principle and Practices - Philadelphia 2018

    Pharmacology - Drug Development Philadelphia (pennsylvania) April 2, 2018 Check with publisher

    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...

  • Biostatistics for Non-Statistician | Salt Lake City Seminar 2018

    Biostatistics for Non-Statistician | Salt Lake City Seminar 2018

    Pharmacology - Drug Development Salt Lake city (Utah) April 2, 2018 Check with publisher

    Course "Biostatistics for the Non-Statistician" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Why should you attend: Statistics is a useful decision making tool in the...

  • Combination Products Regulations Course | USA & EU Seminar 2018

    Combination Products Regulations Course | USA & EU Seminar 2018

    Pharmacology - Drug Development Zurich (Zurich) April 2, 2018 Check with publisher

    Course "Combination Products Regulations: Drug and Device Combinations in the USA and EU" 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 provides...