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Peer Reviewed Papers, Books, Chapters

Year Title Citation Authors
1. 2012 Examination of air and surface particulate levels from cleanroom mats and polymeric flooring European Journal of Parenteral and Pharmaceutical Sciences 2012; 17(3): 110-11
2. 2012 Application of Quality Risk Management To Set Viable Environmental Monitoring Frequencies in Biotechnology Processing and Support Areas PDA Journal of Pharmaceutical Science and Technology, Vol. 66, No. 6, November–December 2012
3. 2012 In vitro Antifungal Efficacy of Biguanides and Quaternary Ammonium Compounds against Cleanroom Fungal Isolates PDA Journal of Pharmaceutical Science and Technology, May/June 2012, Vol. 66, No. 3: 236-242
4. 2012 Isolators in international GMP guidelines Clean Air and Containment Review, Issue 10, pp21-23
5. 2012 A new wave of sporicidal disinfectants Clean Air and Containment Review, Issue 10, pp10-13
6. 2012 Application of Sterilization by Gamma Radiation for Single-Use Disposable Technologies in the Biopharmaceutical Sector Journal of GXP Compliance, Spring 2012
7. 2012 A review of fungal contamination in pharmaceutical products and phenotypic identification of contaminants by conventional methods European Journal of Parenteral and Pharmaceutical Sciences, Vol. 17, No.1: 4-19
8. 2012 Real-time counting of airborne particles and microorganisms: a new technological wave? Clean Air and Containment Review, Issue 9, pp4-6
9. 2011 Some considerations for the implementation of disposable technology and single-use systems in biopharmaceuticals Journal of Commercial Biotechnology, Vol. 17, No. 4: 319–329
10. 2011 Some considerations for the implementation of disposable technology and single-use systems in biopharmaceuticals Journal of Commercial Biotechnology, Vol. 17, No. 4: 319–329 doi: 10.1057/jcb.2011.21
11. 2011 A Review of Cleanroom Microflora: Types, Trends, and Patterns PDA Journal of Pharmaceutical Science and Technology, Vol. 65, No. 4, July–August 2011, pp392-403
12. 2011 Advances in Cleanroom Technology Process India, Vol. 1, No.3, pp42-44
13. 2011 A study of a new type of swab for the environmental monitoring of isolators and cleanrooms (the Heipha ICR-Swab) European Journal of Pharenteral and Pharmaceutical Sciences, Vol. 16, No.2, pp42-48
14. 2011 Two extremes? Flexible working in Europe: A study of differences in Flexible Working Time between two European Plasma Fractionators in Britain and the Netherlands Saarbrucken: VDM Publishing, IBSN 978-3-639-34965-8
15. 2011 Microbial recovery on settle plates in unidirectional airflow cabinets Clean Air and Containment Review, Issue 6, pp8-10
16. 2011 Selection of active air samplers Clean Air and Containment Review, Issue 5, pp8-10
17. 2010 Selection of Microbiological Culture Media and Testing Regimes Saghee, M.R., Sandle, T. and Tidswell, E.C. (Eds.) (2010): Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices, New Delhi: Business Horizons, pp101-120
18. 2010 Environmental Monitoring and Cleanrooms Environmental Monitoring and Cleanrooms, IDMA-APA Guideline, Technical Monograph No.5, Indian Drug Manufacturers Association, Mumbai
19. 2010 Selection of active air samplers European Journal of Parenteral and Pharmaceutical Sciences, Vol. 15, No.4, 2010, pp119-124
20. 2010 Risk Management in Pharmaceutical Microbiology Saghee, M.R., Sandle, T. and Tidswell, E.C. (Eds.) (2010): Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices, New Delhi: Business Horizons, pp553-588
21. 2010 Current Perspectives on Environmental Monitoring Sandle, T. (editor) (2010): Current Perspectives on Environmental Monitoring: Pharmig Review Number 1, Published by Pharmaceutical Microbiology Interest Group, UK. ISBN 978-0-9560804-1-7
22. 2010 Environmental Monitoring Saghee, M.R., Sandle, T. and Tidswell, E.C. (Eds.) (2010): Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices, New Delhi: Business Horizons, pp293-326
23. 2010 Microbial Content Testing of Pharmaceutical and Biotechnologically Derived Products Saghee, M.R., Sandle, T. and Tidswell, E.C. (Eds.) (2010): Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices, New Delhi: Business Horizons, pp327-362
24. 2010 The Media Kitchen: Preparation and Testing of Microbiological Culture Media Sutton, S. (ed.): Laboratory Design: Establishing the Facility and Management Structure, Parenteral Drug Association, Bethesda, MD, United States, ISBN 1-933722-46-0, pp269-293
25. 2010 Best practices in microbiology laboratory training Hodges, N. and Hanlon, G. Industrial Pharmaceutical Microbiology: Standards and Controls, Supplement 11, ppS11.1 to S11.16
26. 2010 Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices Saghee, M.R., Sandle, T. and Tidswell, E.C. (Eds.) (2011): Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices, New Delhi : Business Horizons
27. 2010 The Essentials of Pharmaceutical Microbiology Saghee, M.R., Sandle, T. and Tidswell, E.C. (Eds.) (2010): Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices, New Delhi: Business Horizons, pp1-30
28. 2010 Practical Approaches to Sterility Testing Saghee, M.R., Sandle, T. and Tidswell, E.C. (Eds.) (2010): Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices, New Delhi: Business Horizons, pp173-192
29. 2010 Selection and Validation of Disinfectants Saghee, M.R., Sandle, T. and Tidswell, E.C. (Eds.) (2010): Microbiology and Sterility Assurance in Pharmaceuticals and Medical Devices, New Delhi: Business Horizons, pp219-236
30. 2009 The assessment of air -cleanliness in cleanrooms and cleanzones using optical particle counters The Journal, Institute of Science and Technology, Winter 2009, pp4-7
31. 2009 Best practices for microbiological documentation Industrial Pharmaceutical Microbiology Standards and Controls, Euromed Communications, England, Supplement 9, S9, S9.24
32. 2008 Comparison of dry-heat depyrogenation using three different types of Gram-negative bacterial endotoxin European Journal of Parenteral and Pharmaceutical Sciences, Volume 13, No.1, 2008, pp17-20
33. 2008 A method to determine the effect of dehydration on agar plates and microbial recovery The Institute of Science and Technology Journal, Spring 2008, pp24-27
34. 2007 Selection of Laboratory Disinfectants: Part Two Science Technology Journal, Institute of Science Technology, Spring 2007, pp5-7
35. 2006 Environmental Monitoring Risk Assessment Journal of GXP Compliance, Volume 10, Number 2, 2006, pp54-73
36. 2006 Environmental Monitoring Handbook Sandle, T. and Boschi, F. (2006): Environmental Monitoring Handbook, Advanstar, Duluth, USA (HBEM06). Published in July 2006
37. 2006 Selection of Laboratory Disinfectants: Part One Science Technology Journal, Institute of Science Technology, Summer 2006, pp16-18
38. 2006 The use of polymeric flooring to reduce contamination in a cleanroom changing area European Journal of Parenteral and Pharmaceutical Sciences, Vol. 11, No.3, 2006, pp75-80
39. 2005 Understanding Clean Air Devices Science Technology Journal, April 2005, pp3-5
40. 2005 Examination of the optimal cultural conditions for the microbiological analysis of a cold demineralised water system in a pharmaceutical manufacturing facility European Journal of Parenteral and Pharmaceutical Sciences, Vol. 10, No.1, 2005, pp9-14
41. 2004 Practical Approaches to Sterility Testing Journal of Validation Technology, Vol. 10, No.2, 2004, pp131-141
42. 2004 An Approach for the Reporting of Microbiological Results from Water Systems PDA Journal of Pharmaceutical Science and Technology, Vol. 58, No.4, July-August 2004, pp231 – 237
43. 2004 Gram's Stain: History and Explanation of the Fundamental Technique of Determinative Bacteriology IST Science and Technology Journal, April 2004 (No. 54), pp3-4
44. 2003 The use of a risk assessment in the pharmaceutical industry: the application of FMEA to a sterility testing isolator: a case study European Journal of Parenteral and Pharmaceutical Sciences, 2003; 8(2): 43-49
45. 2003 Selection and use of cleaning and disinfection agents in pharmaceutical manufacturing Sandle, T. Selection and use of cleaning and disinfection agents in pharmaceutical manufacturing in Hodges, N and Hanlon, G. (2003): Industrial Pharmaceutical Microbiology Standards and Controls, Euromed Communications, England (chapter revised on several occasions)


4th Annual Pharma R&D Asia Congress
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