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Best Practice for the Analytical Laboratory - Analytical Methods: Documentation, Validation and Transfer

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Quality Control (QC) laboratories perform a vital role within Good Manufacturing Practice.

Dates: Monday 13 to Tuesday 14 May 2025
Venue:
Manchester Marriott Victoria and Albert Hotel, Manchester, UK
Cost:

£1400.00 excl. VAT – £1680.00 incl. VAT

Type: Pharmaceutical

About this course

Quality Control (QC) laboratories perform a vital role within Good Manufacturing Practice. They provide the data upon which critical decisions, such as batch release and the stability of products, are based. If the laboratory data is incorrect, then decisions may be wrong, with potentially disastrous consequences for companies and patients.

So ensuring the integrity of the data produced by QC laboratories is essential, and a key component in providing data integrity is the validation of the test methods.

This year we have extended our previous one-day course to a two-day course that provides a more detailed explanation of how analytical methods are validated, enabling a full understanding of method performance characteristics and associated statistics, and how they are applied to the techniques used for analysing drug related samples. This knowledge will enable informed interpretation of the regulatory guidance on validation, namely ICH Q2(R1) and guidance from FDA and EMA on bioanalytical methods.

Many organisations encounter difficulties when they attempt to transfer methods from one laboratory to another. This course will provide you with strategies and approaches to ensure success in this complex area.

What You Will Learn

After attending this course you will be able to:

  • Understand the purpose of analytical method validation
  • Define the parameters used for method validation, ie validation characteristics
  • Generate a validation protocol including relevant acceptance criteria
  • Interpret the results of validation using appropriate statistics
  • Understand best practice for analytical method transfer

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