Current Requirements for Cleaning Validation

+ Book Online Now

Course Dates

  • Current Requirements for Cleaning Validation (Virtual)

    5th December 2024 - 6th December 2024

    Location: Virtual Training
    Course Price £1345.00
    Book Now
  • Current Requirements for Cleaning Validation

    We have produced an overview of the course information available online, available here in a handy PDF Prospectus.

    Download Course PDF
Course Terms & Conditions

Cleaning Validation Training Course

Current Requirements for Cleaning Validation is our flagship Cleaning Validation Course.  Validation of cleaning procedures is critical for any cleaning programme as defined in the current GMP Guidelines (Annex 15, Section 10): “Cleaning Validation should be performed in order to confirm the effectiveness of a cleaning procedure for all product contact equipment”

Since the first statement regarding cleaning in the GMP Regulations, the number of guidelines has greatly increased, especially since 2000. This has coincided with the increased focus by regulators within this area.

This pharmaceutical validation course covers topics such as the development of regulatory expectations, effective cleaning procedures, process validation and control of these procedures. It will cover all areas from the inception of a cleaning strategy and policy through the development and performing of the exercise to the maintenance of the validated cleaning regimes.

For those new to this area, this cleaning validation course provides a detailed and structured introduction to cleaning validation, whilst for those who have been working in the field for some time this up to the minute course will provide details of current best practice, cGMP expectations, industry trends and regulatory issues for both the EU and US markets.  It will cover subjects such as development of regulatory expectations, effective cleaning procedures and disinfectant regimes, development of effective cleaning techniques, interactive case studies and the validation and control of these procedures.

Honeyman is renowned for industry leading GMP knowledge-transfer, lectures, consultancy and courses delivered face-to-face and online. Our Training helps stay at the top of your game.

To view our full range of training courses please download the Honeyman Training Prospectus.  Book your place now or enquire about our other Pharma Courses – Honeyman Training

For practical assistance with outsourced monitoring for contamination control in pharmaceutical manufacturing visit

Cleaning Validation Course & Training | Honeyman Group

Who Should Attend This Course?

This validation course will be beneficial for all team members who are involved in performing cleaning validation or managing the process including:

  • Quality Assurance
  • Quality Control
  • Engineering
  • Validation
  • Production or Operations

Course Objectives

Upon completing the course delegates will:

  • Understand the key GMP requirements for cleaning validation and verification
  • Understand the methods of cleaning including manual, automated or COP
  • Be able to develop effective cleaning procedures
  • Understand the significance of product development data in cleaning validation
  • Develop approaches based on scientific rationale
  • Develop protocols, define worst case locations, set limits and define acceptance criteria
  • Apply best practice techniques for direct surface sampling and recovery
  • Understand the suitability and technology associated with specific and non specific analytical techniques
  • Apply risk assessment techniques
  • Understand the importance of maintaining the validation state: cleaning stability studies and change control

Course Content

The course will cover the following:

  • Basics and Approach
  • Documentation
  • Acceptance Criteria
  • Annex 15 Requirements for PDE
  • Sampling and Recovery Analysis
  • Rapid Equipment Cleaning Verification
  • Monitoring Using TOC Analysis
  • Annex 15 Requirements for PDE
  • Stability and Change Control
  • Risk Based Approach to Cleaning Validation and Cross Contamination
  • Case Study Workshop
  • Discussion of Workshop Case Study
  • Interactive Risk Assessment Session
  • Maintenance and Disinfectant Efficacy Status
  • Questions and Answers

Course Dates / Costs Description

Honeyman reserves the right to amend any prices at any time.

All advertised prices are exclusive of any applicable VAT or local taxes.

5th December 2024
Book Now

Training prospectus 2024

We have produced an overview of the course information available online, available here in a handy PDF Prospectus.


Our Customers

Our team has trained and works with the world's leading Pharmaceutical companies, including …

Latest News

3rd May 2024

Virtual training Vs in-Person courses: A Comparison

Read more

23rd April 2024

Technical Briefing (PDF): Liquid and Gas Filtration

Read more

13th February 2024

Locations we cover as a Pharmaceutical Training Company

Read more

30th January 2024

Technical Briefing (PDF): Cleanroom Airflow Visualisation

Read more

15th December 2023

Technical Briefing (PDF): High Efficiency Air Filters

Read more

1st December 2023

Why Attend the Microbial Risk Management During Cleanroom Operations Course?

Read more

17th November 2023

Benefits of Biotechnology Training Course

Read more

29th September 2023

Benefits of Microbiology Course for Non-Microbiologists in Pharmaceutical Manufacturing

Read more

11th September 2023

Benefits of Pharmaceutical Sterilisation Courses

Read more
View all articles