• John C. Fetzer Recorded
    View Anytime
    Price: $190.00
    by: John C. Fetzer
    Analytical Method Validation Under Good Laboratory Practices - GLPs
    If you do any work that will be reported to the US Food and Drug Administration (FDA), Environmental Protection Agency (EPA), or Occupational Safety and Health Administration (OSHA), your work must be done under GLP. All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more.

  • John C. Fetzer Recorded
    View Anytime
    Price: $190.00
    by: John C. Fetzer
    HPLC Analytical Method Development and Validation
    Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals. The focus of most validation work is on the methodology, the standard operating procedure (SOP). But validation of the instrumentation and other associated items of column, solvents, and other reagents and chemicals is also an area of focus in an audit.

  • John C. Fetzer Recorded
    View Anytime
    Price: $190.00
    by: John C. Fetzer
    Analytical Method Validation Under Good Laboratory Practices - GLPs
    If you do any work that will be reported to the US Food and Drug Administration (FDA), Environmental Protection Agency (EPA), or Occupational Safety and Health Administration (OSHA), your work must be done under GLP. All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more.

  • John C. Fetzer Recorded
    View Anytime
    Price: $190.00
    by: John C. Fetzer
    Analytical Method Validation Under Good Laboratory Practices - GLPs
    If you do any work that will be reported to the US Food and Drug Administration (FDA), Environmental Protection Agency (EPA), or Occupational Safety and Health Administration (OSHA), your work must be done under GLP. All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more.

  • John C. Fetzer Recorded
    View Anytime
    Price: $190.00
    by: John C. Fetzer
    Analytical Method Validation Under Good Laboratory Practices - GLPs
    If you do any work that will be reported to the US Food and Drug Administration (FDA), Environmental Protection Agency (EPA), or Occupational Safety and Health Administration (OSHA), your work must be done under GLP. All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more.

  • John C. Fetzer Recorded
    View Anytime
    Price: $190.00
    by: John C. Fetzer
    Analytical Method Validation Under Good Laboratory Practices - GLPs
    If you do any work that will be reported to the US Food and Drug Administration (FDA), Environmental Protection Agency (EPA), or Occupational Safety and Health Administration (OSHA), your work must be done under GLP. All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more.

  • John C. Fetzer Recorded
    View Anytime
    Price: $190.00
    by: John C. Fetzer
    HPLC Analytical Method Development and Validation
    Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals. The focus of most validation work is on the methodology, the standard operating procedure (SOP). But validation of the instrumentation and other associated items of column, solvents, and other reagents and chemicals is also an area of focus in an audit.

  • John C. Fetzer Recorded
    View Anytime
    Price: $190.00
    by: John C. Fetzer
    HPLC Analytical Method Development and Validation
    Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals. The focus of most validation work is on the methodology, the standard operating procedure (SOP). But validation of the instrumentation and other associated items of column, solvents, and other reagents and chemicals is also an area of focus in an audit.

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