Honeyman Group Ltd courses

...works with clients to evaluate, advise upon and develop ongoing environmental monitoring, cleaning validation and disinfectant efficacy programmes... Learn about: Cleanroom Design, RABS and Isolators, HEPA Filters...

...Learn the key points of design, build and operation of pharmaceutical water systems. Water purification, storage and distribution system elements illustrated... Learn about: Reverse Osmosis, Monitoring and Qualification, Pharmaceutical Water Grades...

...but are not qualified microbiologists. Course content includes: The importance of microbiological data and control in pharmaceutical and medical device... Learn about: Sterile Product Manufacture, Interpretation of Data, Bacterial Identification...

...This course covers all key aspects of sterile product manufacture, for both aseptically prepared and terminally sterilised products. New course topics include... Learn about: Risk Management of Contamination, Aseptic manufacture, Inspection Techniques...

...Principles of Moist Heat Sterilisation Steam Quality Generation Distribution and use Dry Heat Sterilisation and Depyrogenation Instrumentation and Control... Learn about: Dry Heat Sterilisation, Pharmaceutical Sterilisation, Pharmaceutical manufacturing...

...Risk Based Approach to Cleaning Validation and Cross Contamination Case Study Workshop Discussion of Workshop Case Study Interactive Risk Assessment Session... Learn about: Effective Cleaning Procedures, Cross Contamination, Risk Assessment...

...most accurate methods of assessing risk, defined as the number of microbes likely to be deposited into a product. All general sources of cleanroom contamination... Learn about: Surface Contact Contamination, Pharmaceutical Products, Cleanroom Manufacture...

...Differences between the production of a variety of cell substrates e.g. mammalian, bacterial, viral, and plant cell products - Upstream processing including cell culture... Learn about: Installation Qualification, Operational Qualification, IQ OQ PQ...

...Heat Sterilisation Steam Quality Generation Distribution and Use Dry Heat Sterilisation and Depyrogenation Instrumentation and Control of Sterilisation...

...is suitable for all personnel involved in cleanroom operation and management, including Engineers, QA, and Validation Course review: Successful cleanroom...

...all involved in the testing of autoclaves adn review of validation data, including technicians, engineers and QA Course review: This course builds on...

...including Engineering, Quality Assurance, Microbiology, QC, Production, Operations and HIgh Purity Water SME's Course review: Water is used throughout the pharmaceutical industry...

...to the highest possible standards expected by the Regulatory Authorities...

...who review data but are not qualified microbiologists. Anyone who works in a sterile manufacturing operation who is not directly involved in microbiology...

...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...

...All personnel involved in or seekingfurther understanding of the inspection process, including technical experts, quality assurance, regulatory affairs...

...This course covers topics such as the development of regulatory expectations, effective cleaning procedures and the validation and control of these procedures... Learn about: Effective Cleaning Procedures, Product contact equipment, Annex 15 Requirements...

...for sterile and non-sterile product manufacture Micro limit testing Monitoring methods: sampling methods, isolation and counting Interpretation of microbiological... Learn about: Gram Positive Bacteria, Regulatory Expectations, Control Measures...