Agilent Training Program for Regulatory Compliance in the Pharmaceutical Industry

This document introduces the training courses provided by Agilent Technologies, including instrumentation qualification, method validation, etc. These courses can help users understand the performance of instruments, validate whether the methods are suitable, etc.


Agilent Training Program for Regulatory Compliance in the Pharmaceutical Industry - cover page
Brand
Agilent
Document type
Other
Language
English
Pages
1
File format
PDF
File size
43 KB
Published
04 July, 2012
Updated
30 September, 2023
MD5 checksum
1A4E0BA3CE1D22C0A6C5275D2A127EF0

About this manual

Agilent Technologies offers carefully planned training courses designed to help users qualify and document the performance of their chemical analysis instruments and systems. These courses ensure instruments meet specifications, methods are up-to-date, and laboratory analyses have traceable records.

The document lists two specific courses: H1183A, a one-day course on instrumentation qualification for LC, GC, GC/MS, IR, and U-Vis instruments, and H1184A, a two-day course on method validation for pharmaceutical applications.

What's inside

  • Training Program
  • Regulatory Compliance
  • Instrumentation Qualification
  • Method Validation
  • Course H1183A
  • Course H1184A
  • Chemical Analysis Instruments
  • Pharmaceutical Laboratories

Frequently asked questions

What is the purpose of the H1183A course?

This course teaches operating principles as well as validation and qualification approaches for LC, GC, GC/MS, IR and U-Vis chemical analysis instruments in pharmaceutical laboratories.

How many days does the H1184A course last?

The H1184A course lasts for 2 days.

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