Edited by Dr. Tim Sandle (established 2010). Applied Biology; a Masters degree in education; and has a doctorate from Keele ). This key part of controlling risk escalation can lead to the contamination of medicinal products, hence necessary tracking precautions are essential. University of Manchester for the university’s pharmaceutical microbiology MSc for pharmaceuticals, Pharmig Adriatic Conference, 21, Best practices with microbiological ls and Le loro, Questo conteggio "Citato da" include citazioni ai seguenti articoli in Scholar. This book offers guidance on building an up to date and complete biocontamination strategy. The chapter on risk management has been extensively revised, especially the section on risk assessment. Tim Sandle discusses career as a Tim Sandle, Head of Microbiology, Bio Products Laboratory Limited, 68 Alexandra Road, London Colney, St. Albans Hertfordshire, UK, Tel: +07-808-906409; E-mail: tim.sandle@bpl.co.uk. practice in environmental monitoring, Assuring the quality of medicines III: Try again later.
Dr. Tim Sandle is an experienced microbiologist, quality professional, auditor and technical writer. 'Fungi in pharmaceutical manufacturing', European Compliance Academy Microbiology Conference, Copenhagen, Denmark, 25th April 2013, 'USP 1116 and its impact upon pharmaceutical microbiology', Pharmig webinar, 1st May 2013, 'The use of control strains for the quality control of culture media', American Pharmaceutical Review Webinar, 14th August 2013 (with Liz Kerrigan of ATCC), 'Hospitals, Water Systems and Contamination, NHS QA Symposium, Chester, UK. Best practices for an environmental monitoring programme, Making Pharmaceuticals, National Motorcycle Museum, Birmingham, U.K. April 28, 2015, Risk assessment and microbiological risks to pharmaceuticals, Making Pharmaceuticals, National Motorcycle Museum, Birmingham, U.K. April 28, 2015, Webinar - Microbiological Risk of Personnel and Cleanrooms - 28th May 2015, Webinar - Disinfection/Sanitisation Processes: cGMP for Cleaning and Disinfection, 25th June 2015, Pharmig - 25th June 2015, The Problem with Spores in Aseptic Units, presented at 'Sporicides – As Part Of Your Transfer Process' - a Pharmig ./ NHS joint symposium, Birmingham, U.K. on 1st July 2015, Sporicidal Products - a problem of definition and control, presented at 'Sporicides – As Part Of Your Transfer Process' - a Pharmig ./ NHS joint symposium, Birmingham, U.K. on 1st July 2015, Environmental control and environmental monitoring, presented at King's College Hospital NHS Trust, London, U.K., on 24th July 2015, Validation of an Agar Plate Active Microbial Air Sampler According to ISO 14698, Merck webinar, 16th September 2015, The future of ISO 14698, Merck webinar, 16th September 2015, Microbiology Laboratory Myths, 10th PDA Global Microbiology Conference, Bethesda, MD, USA, 19th October 2015, Ask the experts panel, 10th PDA Global Microbiology Conference, Bethesda, MD, USA, 19th October 2015, Disinfection Processes for Pharmaceuticals and Surface Sampling on Sanitized Surfaces, Merck webinar, broadcast in Europe and North America (2 sessions) on 22nd October 2015, Bioburden control and objectionable organisms (with Andy Martin), Pharmig Microbiology Conference, Nottingham, U.K., 25th November 2015, Environmental Monitoring Risk Assessment and the Lean Approach, Pharmig Microbiology Conference, Nottingham, U.K., 26th November 2015, Best practices for aseptic operator practice and gowning, Pharmig Microbiology Conference, Nottingham, U.K., 26th November 2015, ISO 14644 Revision to Parts 1 and 2 (2015 updates), Pharmig webinar, 4th February 2016, Overview of environmental monitoring regulations, Pharmig Environmental Monitoring Course, The Oxfordshire Hotel, Oxford, 3rd March 2016, Environmental monitoring incubation strategies, Pharmig Environmental Monitoring Course, The Oxfordshire Hotel, Oxford, 3rd March 2016, Bacterial and fungal spores - aseptic processing risks, Pharmig & NHS Sporicidal Meeting, The Oxfordshire Hotel, Oxford, 4th March 2016, Selection of disinfectants and sporicides, Pharmig & NHS Sporicidal Meeting, The Oxfordshire Hotel, Oxford, 4th March 2016, Environmental monitoring trending for risk mediation and lean manufacturing, PDA Europe, 10th May 2016 - webinar, Environmental monitoring and microflora - key points, ECA Pharmaceutical Microbiology Conference, Barcelona, 11th May 2016, Investigating Sterility Test Failures, Joint Pharmaceutical Analysis Group, Royal Society for Chemistry, London, 12th May 2016, Environmental monitoring incubation strategies, Pharmig Irish Conference, Fota Island Hotel, Cork, 18th May 2016, Best practices in pharmaceutical gowning, at: PHSS Sterile Products Manufacture June 9, 2016, Hallmark Hotel Manchester Airpor, Best practices for investigating sterility test failures, Pharmig webinar, 6th September 206, Depyrogenation Studies, A3P, Lyon, 18th September 2016, Best practices with microbiological culture media, Pharmig 24th Conference, Nottingham, UK, 17th November 2016, Cleanroom contamination; the Problem Spores and the need for Sporicides, Pharmig conference, Wednesday 15th Feb 2017 - Nailcotte Hall Hotel, Berskwell, Warwickshire, Introduction to cleanrooms, Thursday 16th Feb 2017- Nailcotte Hall Hotel, Berskwell, Warwickshire, Current regulations for environmental monitoring, Wednesday 24th May 2017, Pharmig conference, Portmarnock Hotel & Golf Links, Co. Dublin, Ireland, Selecting culture media for environmental monitoring, Wednesday 24th May 2017, Pharmig conference, Portmarnock Hotel & Golf Links, Co. Dublin, Ireland, Approaching depyrogenation, Pharmig webinar, 10th August 2017, ‘Fungal Contamination in Pharmaceutical Products and Cleanroom Risk’, webinar for Pharmig, 4th October 201, Environmental monitoring - limitations, incubating, and trending, 18th October 2017, Pharmig / Samples H conference: Hot Topics in Pharmaceutical Microbiology for the Adriatic Region, Otocec, Slovenia, Training in cleanroom contamination, disinfection, and cleaning techniques, 18th October 2017, Pharmig / Samples H conference: Hot Topics in Pharmaceutical Microbiology for the Adriatic Region, Otocec, Slovenia, How to manage sterility test issues and failure investigations, 18th October 2017, Pharmig / Samples H conference: Hot Topics in Pharmaceutical Microbiology for the Adriatic Region, Otocec, Slovenia, Quantitative determination of endotoxin, Pharmig open discussion session, Pharmig Annual Conference, Oxfordshire, UK, 30th November 2017, Risk Based Approach to Environmental Monitoring, webinar for Compliance Online, 19 December 201, Sterility test failure investigations, webinar for Compliance Online, 23 Jan 2018, Review of EU GMP Annex 1, webinar for Compliance Online, 15 March 201, Introduction to disinfectants for GMP industries, Ecolab webinar, 3 April 2018, Fungi and cleanroom contamination, webinar for Compliance Online, 26 April 2018, Pharmig review of Annex 1, Pharmig webinar, 3 May 201, Bacterial and fungal spore risks to pharmaceutical processing, Webinar, Online Compliance Panel, 23rd May 201, Best practices in microbial culture media, Pharmig Irish Conference, Dublin, Ireland, 30th May 2018, Insight into EU GMP Annex 1, Pharmig Irish Conference, Dublin, Ireland, 30th May 2018, Introduction to FMEA: Risk assessment tool for pharmaceuticals, Pharmig risk assessment course, Dublin, Ireland, 31st May 2018, Good Design Practices For Pharmaceutical Water Systems, webinar, Online Compliance, 28th June 2018, Developing a meaningful
Dr. Tim Sandle is an experienced microbiologist, quality professional, auditor and technical writer. 'Fungi in pharmaceutical manufacturing', European Compliance Academy Microbiology Conference, Copenhagen, Denmark, 25th April 2013, 'USP 1116 and its impact upon pharmaceutical microbiology', Pharmig webinar, 1st May 2013, 'The use of control strains for the quality control of culture media', American Pharmaceutical Review Webinar, 14th August 2013 (with Liz Kerrigan of ATCC), 'Hospitals, Water Systems and Contamination, NHS QA Symposium, Chester, UK. Best practices for an environmental monitoring programme, Making Pharmaceuticals, National Motorcycle Museum, Birmingham, U.K. April 28, 2015, Risk assessment and microbiological risks to pharmaceuticals, Making Pharmaceuticals, National Motorcycle Museum, Birmingham, U.K. April 28, 2015, Webinar - Microbiological Risk of Personnel and Cleanrooms - 28th May 2015, Webinar - Disinfection/Sanitisation Processes: cGMP for Cleaning and Disinfection, 25th June 2015, Pharmig - 25th June 2015, The Problem with Spores in Aseptic Units, presented at 'Sporicides – As Part Of Your Transfer Process' - a Pharmig ./ NHS joint symposium, Birmingham, U.K. on 1st July 2015, Sporicidal Products - a problem of definition and control, presented at 'Sporicides – As Part Of Your Transfer Process' - a Pharmig ./ NHS joint symposium, Birmingham, U.K. on 1st July 2015, Environmental control and environmental monitoring, presented at King's College Hospital NHS Trust, London, U.K., on 24th July 2015, Validation of an Agar Plate Active Microbial Air Sampler According to ISO 14698, Merck webinar, 16th September 2015, The future of ISO 14698, Merck webinar, 16th September 2015, Microbiology Laboratory Myths, 10th PDA Global Microbiology Conference, Bethesda, MD, USA, 19th October 2015, Ask the experts panel, 10th PDA Global Microbiology Conference, Bethesda, MD, USA, 19th October 2015, Disinfection Processes for Pharmaceuticals and Surface Sampling on Sanitized Surfaces, Merck webinar, broadcast in Europe and North America (2 sessions) on 22nd October 2015, Bioburden control and objectionable organisms (with Andy Martin), Pharmig Microbiology Conference, Nottingham, U.K., 25th November 2015, Environmental Monitoring Risk Assessment and the Lean Approach, Pharmig Microbiology Conference, Nottingham, U.K., 26th November 2015, Best practices for aseptic operator practice and gowning, Pharmig Microbiology Conference, Nottingham, U.K., 26th November 2015, ISO 14644 Revision to Parts 1 and 2 (2015 updates), Pharmig webinar, 4th February 2016, Overview of environmental monitoring regulations, Pharmig Environmental Monitoring Course, The Oxfordshire Hotel, Oxford, 3rd March 2016, Environmental monitoring incubation strategies, Pharmig Environmental Monitoring Course, The Oxfordshire Hotel, Oxford, 3rd March 2016, Bacterial and fungal spores - aseptic processing risks, Pharmig & NHS Sporicidal Meeting, The Oxfordshire Hotel, Oxford, 4th March 2016, Selection of disinfectants and sporicides, Pharmig & NHS Sporicidal Meeting, The Oxfordshire Hotel, Oxford, 4th March 2016, Environmental monitoring trending for risk mediation and lean manufacturing, PDA Europe, 10th May 2016 - webinar, Environmental monitoring and microflora - key points, ECA Pharmaceutical Microbiology Conference, Barcelona, 11th May 2016, Investigating Sterility Test Failures, Joint Pharmaceutical Analysis Group, Royal Society for Chemistry, London, 12th May 2016, Environmental monitoring incubation strategies, Pharmig Irish Conference, Fota Island Hotel, Cork, 18th May 2016, Best practices in pharmaceutical gowning, at: PHSS Sterile Products Manufacture June 9, 2016, Hallmark Hotel Manchester Airpor, Best practices for investigating sterility test failures, Pharmig webinar, 6th September 206, Depyrogenation Studies, A3P, Lyon, 18th September 2016, Best practices with microbiological culture media, Pharmig 24th Conference, Nottingham, UK, 17th November 2016, Cleanroom contamination; the Problem Spores and the need for Sporicides, Pharmig conference, Wednesday 15th Feb 2017 - Nailcotte Hall Hotel, Berskwell, Warwickshire, Introduction to cleanrooms, Thursday 16th Feb 2017- Nailcotte Hall Hotel, Berskwell, Warwickshire, Current regulations for environmental monitoring, Wednesday 24th May 2017, Pharmig conference, Portmarnock Hotel & Golf Links, Co. Dublin, Ireland, Selecting culture media for environmental monitoring, Wednesday 24th May 2017, Pharmig conference, Portmarnock Hotel & Golf Links, Co. Dublin, Ireland, Approaching depyrogenation, Pharmig webinar, 10th August 2017, ‘Fungal Contamination in Pharmaceutical Products and Cleanroom Risk’, webinar for Pharmig, 4th October 201, Environmental monitoring - limitations, incubating, and trending, 18th October 2017, Pharmig / Samples H conference: Hot Topics in Pharmaceutical Microbiology for the Adriatic Region, Otocec, Slovenia, Training in cleanroom contamination, disinfection, and cleaning techniques, 18th October 2017, Pharmig / Samples H conference: Hot Topics in Pharmaceutical Microbiology for the Adriatic Region, Otocec, Slovenia, How to manage sterility test issues and failure investigations, 18th October 2017, Pharmig / Samples H conference: Hot Topics in Pharmaceutical Microbiology for the Adriatic Region, Otocec, Slovenia, Quantitative determination of endotoxin, Pharmig open discussion session, Pharmig Annual Conference, Oxfordshire, UK, 30th November 2017, Risk Based Approach to Environmental Monitoring, webinar for Compliance Online, 19 December 201, Sterility test failure investigations, webinar for Compliance Online, 23 Jan 2018, Review of EU GMP Annex 1, webinar for Compliance Online, 15 March 201, Introduction to disinfectants for GMP industries, Ecolab webinar, 3 April 2018, Fungi and cleanroom contamination, webinar for Compliance Online, 26 April 2018, Pharmig review of Annex 1, Pharmig webinar, 3 May 201, Bacterial and fungal spore risks to pharmaceutical processing, Webinar, Online Compliance Panel, 23rd May 201, Best practices in microbial culture media, Pharmig Irish Conference, Dublin, Ireland, 30th May 2018, Insight into EU GMP Annex 1, Pharmig Irish Conference, Dublin, Ireland, 30th May 2018, Introduction to FMEA: Risk assessment tool for pharmaceuticals, Pharmig risk assessment course, Dublin, Ireland, 31st May 2018, Good Design Practices For Pharmaceutical Water Systems, webinar, Online Compliance, 28th June 2018, Developing a meaningful