John C. Fetzer has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers onl iquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry.
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
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.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
Low-level analysis can be very difficult. Basic issues in both qualitative and quantitative analyses will be described.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
In validation, certain requirements are defined by the needs for the data a laboratory generates.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
Most users of GC-MS and LC-MS assume those techniques do many things that the instruments do not do.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
Assessment of the cause for a non-compliance is a structured series of branching questions.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
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.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
Assessment of the cause for a non-compliance is a structured series of branching questions.
John C. Fetzer |
Duration:60 Minutes |
Price: ¤149.00
| View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
People and communications skills are very important in dealing with customers, but have little connection to doing good lab work. This webinar points out some approaches and skills to connect the two areas.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Assessment of the cause for a non-compliance is a structured series of branching questions.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Assessment of the cause for a non-compliance is a structured series of branching questions.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Low-level analysis can be very difficult. Basic issues in both qualitative and quantitative analyses will be described.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
In validation, certain requirements are defined by the needs for the data a laboratory generates.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
Most users of GC-MS and LC-MS assume those techniques do many things that the instruments do not do.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
People and communications skills are very important in dealing with customers, but have little connection to doing good lab work. This webinar points out some approaches and skills to connect the two areas.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Assessment of the cause for a non-compliance is a structured series of branching questions.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
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.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Instrumental liquid chromatography is an analysis are widely used to determine purity, the impurities, and the degradation products of pharmaceuticals.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Assessment of the cause for a non-compliance is a structured series of branching questions.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Low-level analysis can be very difficult. Basic issues in both qualitative and quantitative analyses will be described.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
In validation, certain requirements are defined by the needs for the data a laboratory generates.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details
Most users of GC-MS and LC-MS assume those techniques do many things that the instruments do not do.
Speaker: John C. Fetzer | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details