Aseptic Processing: Principles in Practice® - Ireland

Download Course PDF Aseptic Processing

It is well understood that sterility of an aseptic product cannot be determined by direct assessment of the finished product. Therefore, microbiological safety of the product can only be achieved by careful assessment of the hazards and control measures in place to provide the confidence that the items are safe for the patient and fit for use.

Historically aseptic processes have relied heavily on monitoring of the environment, air, surfaces and personnel to verify the success of the process. However, modern aseptic processes require a more holistic assessment of all the protective measures in place within the process and the complex interaction between these control measures, this approach is fully covered within this course.

We guarantee that on completion of this course, with the knowledge gained, you will look at aseptic processing from a new perspective. 

Who Should Attend This Course?

This course is suitable for all members of staff working with aseptic processes in sterile product manufacturing operations, including:

  • QP’s and Quality
  • Operational Managers
  • Operations Personnel
  • Technical and Engineering
  • Validation

Course Features

   +   Aseptic Processing Training Risk Assessment   =    Aseptic Process Training Success

Knowledge + Risk Assessment = Success of an Aseptic Process

Full course notes are provided and a certificate of attendance will be issued to each delegate who attends the full course. Certification is for knowledge gained not just attendance.

Course Objectives

  • To understand the fundamental mechanisms of contamination transfer from source to product and the protective measures in place to prevent product contamination.
  • To have the opportunity to work with risk management techniques like HACCP and RMC through practical workshops
  • To understand the technology associated with cleanrooms and aseptic processes and understand the key control measures and they impact the sterility assurance of the product
  • To introduce new thinking for validation and risk assessment of the process
  • To understand the cGMP regulations and guidelines for aseptic processing and to engage in discussions regarding industry changes and best practice. 

Course Content

The course programme includes:

  • Risk Assessment in Aseptic Processing
     - HACCP and RMC Techniques 
  • Pharmaceutical Microbiology
  • Environmental Monitoring
     - Viable, Non-viable particles
  • Bioburden Control & Sterility Assurance
  • Methods of Sterilisation
     - Moist Heat (Porous loads, SIP)
     - Filtration
     - Dry Heat
  • Methods of Decontamination - VHP
  • Clean Utilities - WFI
  • Cleanroom Design and Operation
  • HEPA Filters 
  • RABS & Isolator Technology 
  • People as a Source of Contamination
  • Effective Contamination control
  • Aseptic Validation
  • Process Simulation Tests 
  • Aseptic Processing Guidelines and Regulations
  • Regulatory Trends and Interpretations 

Course Dates / Costs Description

Please see the table above for the dates of next courses and the costs.

Please note: Our online booking system works in £GBP. The € Euro price is a guide price only. The final € Euro amount payable online will be the current exchange rate of the £GBP amount.

If you wish to raise a purchase order or pay via any other means than Credit Card for a booking then these € Euro guide prices will prevail as being the booking cost despite any fluctuation in exchange rates.

Honeyman reserves the right to amend any prices at any time. All advertised prices are exclusive of any applicable VAT or local taxes.

Course Terms & Conditions

Click here to read our Aseptic Processing Training Course Terms & Conditions.

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Aseptic Processing: Principles in Practice® - Ireland

Why Honeyman?

The Honeyman Group has trained thousands of people within the pharmaceutical industry. Our courses continue to remain popular because they provide delegates with a sound understanding of scientific principles in each technical area, complemented by interactive workshops, discussions, practical demonstrations and case studies to put these principles into practice.

All of our courses are delivered by experts who actively work within the pharmaceutical, biopharmaceutical and medical device industries, therefore, we will continue to share pragmatic current best practice advice to enable you to meet current GMP and regulatory expectations.

  • Our speakers are active in the industry today and are able to provide up to the minute experiences and current best practice advice
  • Accredited Specialist Training on selected courses in conjunction with Teesside University
  • We can provide bespoke on site training, perfectly suited to deliver the most effective and relevant training

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