Honeyman Group Ltd courses

...Working with many of the world’s leading pharmaceutical and medical device manufacturers, the Honeyman Group is currently involved with a number of cleanroom... Learn about: RABS and Isolators, HVAC Systems, Cleanroom Design...

...Learn the key points of design, build and operation of pharmaceutical water systems. Water purification, storage and distribution system elements illustrated... Learn about: Purified Water, Water Types, Water for Injection...

...Training Course delegates will: • Develop a sound understanding of basic pharmaceutical microbiology • Be able to identify microbial hazards • Learn how... Learn about: Regulatory Expectations, Microbiology in Manufacturing Processes, Bacterial Identification...

...control points for bio burden control in a typical aseptic process Sterilisation steps including terminal sterilisation Sterilisation processes for irradiation... Learn about: Clean Rooms, Inspection Techniques, Auditing QC Laboratories...

...engineering to ensure reliability in full compliance with all European and US regulatory requirements. Key learning objectives of the course... Learn about: Steam Quality, Control Processes, Aseptically Prepared Products...

...for cleaning validation and verification - Understand the methods of cleaning including manual, automated or COP - Be able to develop effective cleaning procedures... Learn about: Recovery analysis, Product contact equipment, TOC Analysis...

...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: Critical Area Contamination, Aseptically Manufactured Products, Risk Management of Contamination...

...of biotechnology management and control. This session will review the standard commonalities and also the specific differences and activities within biotechnology... Learn about: Performance Qualification, Raw Materials, Installation Qualification...

...Biological Indicators Validation Strategies for Sterilisation Processes Routine Operation of Sterilisers Continual Compliance Assurance...

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

...from industry experts. The course includes a refresher on the principles of moist heat sterilisation and the test methods used to demonstrate performance...

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

...system along with risk management, design review, change management and continuous improvement in pharmaceutical manufacturing. The purpose of this course...

...the manufacturing process is a key success factor for production. Microbiology is unseen and data is history, effective control requires all disciplines...

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

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

...Suitable for: The course will be beneficial for newcomers and experieinced personnel from QC, Validation, Engineering, Production and QA. Upon completing... Learn about: CGMP Expectations, Risk Assessment, Cross Contamination...

...to microbiology so that they can engage in the required control measures, investigations and corrective actions. At our Microbiology for Non-Microbiologists... Learn about: Limit Testing, Pharmaceutical Manufacture, Reading Plates...