Honeyman
Training
Honeyman offers 5 training opportunities:
Microbial Risk Management During Cleanroom Operations
Short course (Durham and Varies) by Honeyman · £1195
The course will provide a basic understanding of the Risk Management of Contamination (RMC) system that can be utilised for the control of contamination during manufacturing operations in cleanrooms.
Critical Factors for Sterile Product Manufacturing
Short course (Durham and Varies) by Honeyman · POA
The manufacture of sterile products is subject to additional GMP controls and relies heavily on the competency and knowledge of everyone involved in the process. This course covers all key aspects of sterile product manufacture, for both aseptically prepared and terminally sterilised products.
Cleanrooms: Principles in Practice
Short course (Durham and Varies) by Honeyman · £1560
This Cleanroom Training course provides a holistic view of the design, operation and management of cleanrooms.
Aseptic Processing: Principles in Practice
Short course (Durham and Varies) by Honeyman · £1560
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.
Current Requirements for Cleaning Validation
Short course (Durham and Varies) by Honeyman · POA
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"