Foundation knowledge element of the UK Study Guide

What the QP needs to know and how it all works in practice

  • Key topics

    What, when, where, and why we use stats in Pharma

    Pharma maths and stats, the basics

    Comparison of data, basic tools

    Graphs and charts - data analysis and trending

    Introduction to probability and confidence

    Sampling plans / Acceptable Quality Levels

    Process control and monitoring

    Correlation and regression

    Stats for qualification and validation

    Application to Annual Product Quality Reviews

  • Main Tutors

    Alex Hall

    _____________________________

  • Included

    Application of statistics to process, equipment and method validation

    Workshops, exercises, assessment

    Leadership for the QP

    Form and viva practice

Learning outcomes

You will learn the key elements of what the Qualified Person needs to know to be able to ensure that protocols, reports and data analysis presented to them has used the appropriate statistical approach, methods, calculations and acceptance criteria.
We can't make you a statistician, we can help you spot glaring discrepancies.

  • Key statistical techniques for the Qualified Person, including:
    # Comparison of data, e.g. Correlation, student t-test etc.
    # Statistical process control, e.g. Shewhart charts, CpK / PpK
    # Trending, e.g. Regression analysis, Key Performance Indicators
    # Sampling plans, e.g. how to use ISO 2859

  • Applications of key statistical techniques, including:
    # Product Quality Reviews
    # Quality System and performance metrics
    # Sampling and testing
    # Validation and qualification
    # Storage and distribution, e.g. Temperature mapping studies
    # Determination of hold times / product shelf life
    # Process monitoring / continuous process verification

  • Key guidelines related to the evaluation of data in pharmaceutical manufacture, testing and distribution, including:
    # ICH Q1; Q2; Q8; Q11; Q14
    # GMP Annex 15; Associated Regulatory and industry guidance on validation
    # EP / BP / USP as applicable

  • Note that practical, worked examples will be included in the course to demonstrate the techniques described above
    # The majority of these can be determined in a simple excel spreadsheet

In this portal

Your materials, assignments and assessments will all be provided through this learning portal

You will be notified by email when items are available for you to access...

  • 1 month before the course start date
    ~ You can access your course workbook
    ~ You will be able to download your Preparatory Assignment

  • Day before course start date
    ~ Downloads for workshops and exercises

  • End of each course day
    ~ Answers to exercises where appropriate

  • After course
    ~ Learning assessment
    ~ Course evaluation
    ~ Certificate

How to join us

You will each be sent an invite to join the course via Teams

Our experts will facilitate the group

Easily accessible for you - just follow the link you have been sent

Want to know more, find out about the discount bundles available, or book your training

Call us directly on
01622 477781
email us
[email protected]
or pop your email in the box below and we will get right back to you

Thank You