Honeyman Group Ltd courses

...to define system boundaries and identify critical components - Be able to present a cost-effective approach to validation - Appreciate cleaning and maintaining control... Learn about: Pharmaceutical Clean Room, Environmental Monitoring, Cleanroom Design...

...and biopharmaceutical water systems from the following disciplines: Engineering, Quality Assurance, Microbiology, QC, Production, Operations and high purity water SME’s... Learn about: Pharmaceutical Water Grades, Reverse Osmosis, Monitoring and Qualification...

...to microbiology so that they can engage in the required control measures, investigations and corrective actions. At our Microbiology for Non-Microbiologists... Learn about: Bacterial Identification, Regulatory Expectations, Microbiology in Manufacturing Processes...

...Understand how the key aspects of the facility design, personnel, material flows, aseptic behaviours determine the success of aseptic processing... Learn about: Regulatory Trends, Sterile Product Manufacture, Auditing QC Laboratories...

...Principles in Practice® course provides delegates with a comprehensive understanding of moist heat and dry heat sterilisation processes from theoretical... Learn about: Pharmaceutical Management, Pharmaceutical manufacturing, Pharmaceutical Sterilisation...

...Understand the importance of maintaining the validation state: cleaning stability studies and change control Both new and experienced personnel from... Learn about: Cleaning validation, Cross Contamination, Rapid Equipment Cleaning...

...The course will provide a basic understanding of the Risk Management of Contamination (RMC) system that can be utilised for the control of contamination... Learn about: Pharmaceutical manufacturing, Clean Room, Cleanroom Manufacture...

...and techniques for the process, CQA/CCP, media production and hold times plus cleaning. Validation 2: An overview of the validation and qualification requirements... Learn about: Operational Qualification, Clinical Batches, Performance Qualification...

...Processes Steam In Place Quality Systems Associated with Sterilisation Processes Auditing Sterilisation Processes and Preparing for a Regulatory Inspection...

...of understanding clean room operations is to be involved in hands on exercises, demonstrations and workshops, therefore this course will be reinforced...

...Sterilisation Principles in Practice course by giving delegates the opportunity to receive hands on tuition in the practical aspects of autoclave validation...

...recieved for many years by personnel involved in the design, management and operation of pharmaceutical and biopharmaceutical water systems...

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

...This course is designed to give non-Microbiologists a comprehensive introduction to Microbiology so that they can engage in the required control measures...

...This course covers all key aspects of sterile product manufacture, for both aseptically prepared and terminally sterilised products. This course will involve...

...inspection deficiencies and provide case studies on current GMP issues. This course will give you the opportunity get involved in an open discussion with our industry experts...

...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... Learn about: Product contact equipment, Disinfectant Efficacy, CGMP Expectations...

...Controlling microbiology throughout the manufacturing process is a key success factor for production. Microbiology is unseen and data is history... Learn about: Gram Negative Bacteria, Regulatory Expectations, Bacterial Identification...