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Basic HPLC Theory and Method Development

  • Training

  • Compliance Online
  • ID: 5975990
This HPLC theory (high performance liquid chromatography) training will cover the beginnings of HPLC through method validation and method development. Attention will be paid to understanding the thought process behind HPLC theory methods in the laboratory.

HPLC is a form of separation science that is arguably the most utilized form of analytical chemistry in the pharmaceutical industry. Yes, it is only a tool, but a powerful one that when used properly may be the workhorse QC technique or the sensitive and adaptable R&D system. This webinar will cover the begininnings of HPLC through method validation and method development. Attention will be paid to understanding the thought process behind HPLC methods in the laboratory. Also covered will be how it has been affected by and affected FDA and ICH guidelines.

Areas Covered in the Seminar:

How do you make a method and why are so many monographs combersome at best?

What is HPLC and how did it come about?

What are the pieces/parts of an HPLC system?

How do you chose a column?

What information needs to be captured, recorded, kept and why?

The basics of method validation.

Why does pH and buffers matter?

What are some FDA rules and ICH guidelines?

Who Will Benefit:

This web seminar will train or refresh the partisipant in how HPLC works, why and what are the guidelines affecting the use of HPLC. Regulated companies in the pharmaceutical, biotechnological, and medical device industries will benefit from the webinar presentation. The people that will benefit the most include:
  • Scientists
  • QA managers and personnel
  • QC managers and personnel
  • Validation specialists
  • Consultants
  • Quality system auditors and vendor auditors

Course Provider

  • Jeff Phillips
  • Jeff Phillips,