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Synbiosis: Protocol 2 Is Upgraded To Offer Faster Route For Determining Effectiveness Of Vaccines And Anti-Microbials
12/4/2009 11:48:52 AM
Cambridge, UK: Synbiosis, a world-leading manufacturer of automated microbiological
systems, today announced its ProtoCOL 2 system for colony counting
and inhibition zone analysis has been upgraded to allow rapid statistical analysis
of flu and bacterial vaccine potency and antibiotic susceptibility testing results.
Integral to the Synbiosis ProtoCOL 2 colony counter and zone measurement
system, the ProtoCOL 2 software has been upgraded so numerical data can be
automatically transferred into programmes for statistical analysis to produce ED50
calculations as well as parallel line, slope ratio, Probit, 4-parameter logistic curve
and single dose models. This innovation will save scientists valuable time, as data
can be transferred via a single button click rather than manually entered.
The ProtoCOL 2 system’s simple user interface has also been designed to include
provisions for electronic signatures; a full audit history of both image and written
data and different permission levels for secure access to the data. This ensures
the software can be integrated into any 21 Code of Federal Regulations (CFR),
Part 11 environment, making the ProtoCOL 2 an ideal system for use in a GMP
(Good Manufacturing Practice) compliant facility.
Martin Smith of Synbiosis commented: “With the increased demand for swine flu
vaccines and antibiotics to treat pneumococcal infections, pharma and biotech
firms are under pressure to dispatch these to market quickly. One method of
shortening the delivery timeline is to accelerate testing and release of these
products.”
Martin Smith continued: “This is why we are delighted Synbiosis’ technical team
has identified the transfer of data for analysis as a bottle neck and spent
considerable time and effort developing software that can overcome this
challenge. Their excellent advances ensure pharma companies can now install and begin using a ProtoCOL 2 system for clinical quality assurance, safe in the knowledge
that they can easily obtain accurate efficacy data, which will help them deliver their
vaccines and anti-microbial therapies into hospitals and pharmacies more rapidly.”
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