MicroVal certifies GreenLight TVC method
Automatically detects microbial contamination in food and drink samples
Based in The Netherlands, MicroVal validates and certifies alternative microbiological analysis methods according to EN-ISO 16140.
“After a successful launch in the US, the MicroVal certification will now enhance our ability to market GreenLight series instrumentation across Europe,” says Richard Fernandes, chief executive of Luxcel Biosciences, based in Cork, Ireland, which developed the GreenLight technology.
“The rigorous independent testing that this methodology has gone through over the past two years gives European food processors the confidence to convert to faster, more efficient technology.”
US instrumentation specialist Mocon has marketed the GreenLight technology in the US since 2010. AOAC International, in Gaithersburg, MD, which provides validation and conformity assessment of commercial and analytical methods, previously qualified the methodology.
As part of the MicroVal certification process, the microbial contamination methodology was tested at eight independent laboratories in five different European countries.
The GreenLight series provides same-day results in a cost-effective manner. Depending on the bacterial load, results can be obtained between minutes and 12 hours. This is more than ten times faster than the traditional agar plate or film methods, which typically require 48 to 72 hours to achieve a meaningful microbial count, says Mocon. Shorter testing cycles provide packers and processors with the potential to get their perishable food items to the consumer faster.
The GreenLight 910, 930 and 960 are available to handle a variety of throughput requirements. The series also targets company and laboratory microbial contamination testing requirements for seafood, dairy and produce.
You may also like
Trending Articles
-
You need to be a subscriber to read this article.
Click here to find out more.
Upcoming event
You may also like
Cleaning
Bausch+Lomb has chosen Steriline to improve the production of sterile ophthalmic medical devices
Because Steriline’s line is compliant with the recommendations of the latest version of Annex 1, Bausch+Lomb can expand its production capacity while simultaneously minimising the risks of microbial, particulate and endotoxin/pyrogen contamination in its eye care products
Cleaning
UK wet wipe ban starting 2027: Cleanroom and medical wipes exempt under professional-use rules
Kay Goddard of Antistat & Integrity Cleanroom explains why plastic-containing wipes used in controlled environments will fall outside the consumer ban, and what businesses must do to remain compliant
Containment
Guardtech, STERIS, Kemtile and more: Experts to deliver latest research and insights - plus save £50 with early bird tickets until 23 March
The #1 conference is back with this year’s edition shaping up to be the most consequential yet with deeper technical insight, sharper conversations and a renewed focus on the challenges shaping the future of controlled environments