QP Analysis and Testing 2024
03 - 05 Dec 2024
The testing that a pharmaceutical product undergoes throughout its production needs to be reliable and provide accurate and meaningful answers.
This course provides the aspiring QP with the background and technical knowledge to be able to assure through oversight that the testing meets these criteria.
Learn about the various key activities conducted by the Quality Control laboratory, including:
# Sampling and sample management
# Routine finished product testing
# Method and cleaning validation testing
# Storage and analysis of routine stability samples
# Stability studies to determine product shelf life
# Evaluation and reporting of results
Gain an overview of the key analytical techniques used in the quality control laboratory, including:
# Chromatography (inc HPLC)
# Spectroscopy
# Titrimetric / Gravimetric
Electrochemical, e.g. pH
Understand the requirements for analytical method development and method validation
# As outlined in the updated ICH Q2 and new ICH Q14
Understand the requirements of Good control Laboratory Practice (GcLP), including:
# Documentation control
# Management of Pharmacopeial monographs and methods
# Management of OOS/OOT/OOE results
# Data Integrity
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
Location: Maidstone Innovation Centre,
Gidds Pond Way, Weavering, Maidstone, Kent ME14 5FY
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