Cleanroom Technology Conference 2020: Agenda

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Wednesday 28th October

Time Regulation and Standards Speaker  
08:00 – 09:20 Registration  
09:10 – 09:20 Welcome address from chairman Gordon Farquharson
MD of Critical Systems
Director & Principal Consultant.
Chair of LBI/30, CEN TC243, and
Convenor of ISO T2019 WG1
09:20 – 10:00 KEYNOTE ADDRESS
Meaningful cleanroom environmental monitoring and EU GGMP Annex 1 considerations
Tim Eaton
Effective environmental monitoring
Sterile Manufacturing Specialist
ASTRAZENCA
10:00-10:35 Designing learning programmes to address disinfectant residues in cleanroom per GMP Annex 1 Karen Rossington
CONTEC
10:35-11:10 Debates and challenges concerning disinfectant validation and methods to circumvent them Jim Polarine
STERIS life sciences
11.00 BREAK – MEET THE EXHIBITORS  
11:30-12:05 Attrition of Microbes without Microbiocides in Closed Cell Processing Systems Dr Alicia Henn
Biosperix
12:05-12:40 Microbiological Considerations in Cleanroom Manufacturing Adèle Gisselmann
Merck
13.10-14:20 LUNCH – MEET THE EXHIBITORS  
14:20-14:55 Microbiological Monitoring: How to make the most of your data!

Andrew Davies
Microgenetics
14:55-15:30 ISO Cleanroom Standards Update Part 3: Filters testing. HEPA vs ULPA filters

Gordon Farquharson
MD of Critical Systems,
Director & Principal Consultant.
Chair of LBI/30, CEN TC243, and
Convenor of ISO T2019 WG1
15.30-16:00 Designing and implementing a real time monitoring system – what is right for my cleanroom Les Dodd
EMS
16.00-16:30 BREAK – MEET THE EXHIBITORS  
16:30-17:00 Advances in Hepa Filtration Alan Sweeney
European Clean Process
Segments Manager
Camfil
17:00-17:30 Industry 4.0 and Lean processing workflows in Cleanrooms Helen Tebay
Business Development co-ordinator
Connect 2 Cleanrooms
17.30 – 19.00 Networking & Awards Evening

Thursday 29th June

Time Cleanroom Design & Operations Speaker  
08.30-09:00 Registration  
09.00-09:10 Welcome address from chairman To be confirmed
09:10-09:50 KEYNOTE: Super Cleanrooms! Challenges of creating cleanrooms fit for purpose To be confirmed
09.50-10:25 Application and use of modular cleanrooms and facility design in line with current manufacturing trends George Walker
Business Manager
Ardmac
10.25-11:00 Traditional construction vs new construction techniques, benefits & considerations for a new design approach Lee Harvey
Asgard
11.00-11:20 BREAK – MEET THE EXHIBITORS  
11:20-11:55 Commissioning, verification and testing of cleanrooms and clean zones Stephen Ward
Validair
11:55-12:20 Designing the world’s best disinfectant David Keen
Director Pharmaceutical Microbiology
at EcoLab/Pharmig
12.20-13:00 Disinfectants: balancing all the considerations James Tucker
Technical Service Manager
Redditch
13:00-14:10 LUNCH – MEET THE EXHIBITORS  
14.10-14:45 RABS vs. Isolator – status quo and a look ahead into the future Matthias Angelmaier
Syntegon Technology
14.45-15:20 Optimising and maximise sustainability using air filtration and air change rates within a cleanroom environment. Sean O’Reilly
AAF
15:20-15:50 How to improve quality and compliance, whilst reducing energy consumption, carbon emissions and cost

Keith Beatie
Technical Advisor
The Contamination Control Network
16.55 Q&A and CLOSE DAY TWO