Sponsored by: Contec and Dupont
CHAIRMAN: James Drinkwater, Chairman, Pharmaceutical & Healthcare Science Society
Addressing the Microbiological Aspects in Cleanroom Design and Engineering
SMi Group are pleased to announce the Inaugural Pharmaceutical Cleanroom Technology Europe Conference, taking place on the 9th and 10th October 2019 in London, UK. As the first event in Europe that focuses on cleanroom technology in the pharmaceutical industry, the conference will serve to bridge that gap between the two areas while simultaneously providing a unique selling point.
This one-of-a-kind meeting will facilitate networking opportunities with key opinion leaders from all areas of pharmaceuticals, biologicals, and cleanroom industry experts to explore hot topics within cleanroom design and engineering, best practices and regulation, environmental and contamination control, and pharmaceutical microbiology.
In 2025, the global cleanroom technology market is expected to reach nearly $5 billion. Stringent regulatory standards for product approvals, technological advancements in cleanrooms, initiatives taken by private organisations to create awareness regarding cleanroom and growth of the healthcare sector globally are among the few factors expected to drive the market.
Compliance with the standards for product approvals is crucial and as a result manufacturing companies in various industries are dependent on cleanroom technology.
BENEFITS OF ATTENDING
EXPLORE the characteristics and relevance of air flow to better advise cleanroom design, engineering and manage contamination
DISCUSS the most current approaches to minimised cost and improved energy efficiency without compromising product quality
EXAMINE the latest contamination control strategies from leaders in the pharmaceutical industry
GAIN insight into cleaning and disinfection protocols from a risk-management approachPLUS AN
INTERACTIVE HALF DAY PRE-CONFERENCE WORKSHOP
Tuesday 8th October 2019, Copthorne Tara Hotel, London, UK
Environmental Classification, Qualification and Monitoring of GMP Controlled areas referencing ISO 14644-1 and risk based GMP
Workshop Leader: James Drinkwater, Chairman, Pharmaceutical and Healthcare Science Society
WHO SHOULD ATTEND?
Senior Micro Manager, QC Manager, Quality Director, Clean Room Design Managers, Design, Qualify and Testing - Clean Room (across the board), Head of Clean Room Technologies, Head of Compounding Pharmacies, Head of Clinical Drug Products, Head of Clinical Medical Device
Global Presence: Attendees from all over the world attend our events. Gain hands on insight from representatives from UK, Europe and USA.
EARLY BIRD-RATES
BOOK BY 30th AUGUST AND SAVE 拢200
CHAIRMAN: James Drinkwater, Chairman, Pharmaceutical & Healthcare Science Society
Addressing the Microbiological Aspects in Cleanroom Design and Engineering
SMi Group are pleased to announce the Inaugural Pharmaceutical Cleanroom Technology Europe Conference, taking place on the 9th and 10th October 2019 in London, UK. As the first event in Europe that focuses on cleanroom technology in the pharmaceutical industry, the conference will serve to bridge that gap between the two areas while simultaneously providing a unique selling point.
This one-of-a-kind meeting will facilitate networking opportunities with key opinion leaders from all areas of pharmaceuticals, biologicals, and cleanroom industry experts to explore hot topics within cleanroom design and engineering, best practices and regulation, environmental and contamination control, and pharmaceutical microbiology.
In 2025, the global cleanroom technology market is expected to reach nearly $5 billion. Stringent regulatory standards for product approvals, technological advancements in cleanrooms, initiatives taken by private organisations to create awareness regarding cleanroom and growth of the healthcare sector globally are among the few factors expected to drive the market.
Compliance with the standards for product approvals is crucial and as a result manufacturing companies in various industries are dependent on cleanroom technology.
BENEFITS OF ATTENDING
EXPLORE the characteristics and relevance of air flow to better advise cleanroom design, engineering and manage contamination
DISCUSS the most current approaches to minimised cost and improved energy efficiency without compromising product quality
EXAMINE the latest contamination control strategies from leaders in the pharmaceutical industry
GAIN insight into cleaning and disinfection protocols from a risk-management approachPLUS AN
INTERACTIVE HALF DAY PRE-CONFERENCE WORKSHOP
Tuesday 8th October 2019, Copthorne Tara Hotel, London, UK
Environmental Classification, Qualification and Monitoring of GMP Controlled areas referencing ISO 14644-1 and risk based GMP
Workshop Leader: James Drinkwater, Chairman, Pharmaceutical and Healthcare Science Society
WHO SHOULD ATTEND?
Senior Micro Manager, QC Manager, Quality Director, Clean Room Design Managers, Design, Qualify and Testing - Clean Room (across the board), Head of Clean Room Technologies, Head of Compounding Pharmacies, Head of Clinical Drug Products, Head of Clinical Medical Device
Global Presence: Attendees from all over the world attend our events. Gain hands on insight from representatives from UK, Europe and USA.
EARLY BIRD-RATES
BOOK BY 30th AUGUST AND SAVE 拢200
