Webinar Search Results : 3 Upcoming webinars found.
John C. Fetzer Monday, July 22, 2019
10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Price: $150.00
by: John C. Fetzer
How to Deal With Bad Results Under GLP
Assessment of the cause for a non-compliance is a structured series of branching questions. The answers to these eliminate possibilities and eventually highlight a root cause. This process is described, including roles and responsibilities, timing, and efforts at prevention.

John C. Fetzer Monday, August 12, 2019
10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Price: $150.00
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 Wednesday, August 28, 2019
10:00 AM PDT | 01:00 PM EDT
Duration:60 Minutes
Price: $150.00
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
    Duration:60 Minutes
    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
    Duration:60 Minutes
    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
    Duration:60 Minutes
    Price: $190.00
    by: John C. Fetzer
    How to Deal With Bad Results Under GLP
    Assessment of the cause for a non-compliance is a structured series of branching questions. The answers to these eliminate possibilities and eventually highlight a root cause. This process is described, including roles and responsibilities, timing, and efforts at prevention.

  • 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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