The latest innovation in rapid microbiology method (RMM) instrument technology is real-time viable detectors, like TSI’s BioTrak™ Real-Time Viable Particle Counter. This technology provides unique benefits for microbial contamination monitoring.
The BioTrak Particle Counter has three distinct measurement capabilities, providing maximum awareness of particulate levels present in manufacturing clean room environments. It measures total particulate count by incorporating an ISO-21501-4 compliant optical detection engine based on TSI’s field proven AeroTrak™ Airborne Particle Counters.
Particle viability is determined using TSI’s patented LIF technology developed over the past 20 years in TSI’s biological threat detection products, but optimized for the pharmaceutical application. The BioTrak Particle Counter uses two channels of fluorescence along with particle size in its discrimination of particles to better differentiate between viable particles from non-viable particles.
The BioTrak Particle Counter incorporates all this capability into a single product operated through an intuitive Graphical User Interface containing the features found in modern Airborne Particle Counters.
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GlaxoSmithKline plc and Human Genome Sciences announced that the companies have entered into a definitive agreement under which GSK will acquire HGS for USD14.25 per share in cash. The transaction values HGS at approximately USD3.6 billion on an equity basis, or approximately USD3 billion net of cash and debt, and represents a premium of 99% to the HGS closing price of USD7.17 per share on 18 April 2012, the last day of trading before HGS publicly disclosed GSK’s initial private offer.
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ACHEMA 2012 - Exclusive video interviews
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Conferences, events & exhibitions:
Drug Discovery & Diagnostic Development Week 2012
1 - 3 August 2012 San Francisco, CA, USA
Drug & Diagnostic Development
6 - 8 August 2012 San Francisco, CA, USA
Genomics Research Europe
4 - 5 September 2012 Frankfurt, Germany
ELRIG Drug Discovery 2012
5 - 6 September 2012 Manchester, UK
HUPO 11th Annual World Congress
9 - 12 September 2012 Boston, USA
Design Control for Medical Device Professionals
10 - 11 September 2012 Berlin, Germany
Design Validation, Verification, and Risk Analysis for Medical Device Professionals
12 - 13 September 2012 Berlin, Germany
Validation of Computer Systems
17 - 18 September 2012 Dublin, Ireland
The EU Clinical Trial Directive
17 - 18 September 2012 Dublin, Ireland
ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
17 - 19 September 2012 Dublin, Ireland
The Drug Development Process – From Discovery to Commercialisation
19 - 21 September 2012 Dublin, Ireland
11th Annual Biological Production Forum 2012
24 - 26 September 2012 Dusseldorf, Germany
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