Faster
Validation Results in 60 seconds
Enzyme Indicators are the only advanced validation tool in measuring rapid gaseous bio-decontamination in around 60 seconds per indicator, compared to the 7 day incubation period with traditional methods – measuring performance instantly, reducing cost, saving time, improving efficacy. Resulting in faster product release, immediate batch verification.
Safer
100% Assurance
Performance
The quantifiable results enable optimisation of cycle design and bio-decontamination efficacy on multiple surface types challenge points simultaneously. Enzyme Indicator technology completely alleviates the risk of false positive results and routine cycle failures that impact production – allowing you to be fully confident in your bio-decontamination validation.
Smarter
Real-Time Quantifiable Data
Athena, our bespoke software is used alongside Enzyme Indicators to deliver advanced reporting capability, enhanced audit and review features along with data archive facilities during validation cycles and the delivery of ‘challenge area’ batch specific decontamination data that can be stored electronically reducing the risk of manual data records.
Sectors We Operate In
Pharmaceuticals
Pharmaceuticals Rapid validation for bio-decontamination. Enzyme Indicators offer benefits in the following core pharmaceutical disciplines such as Technical (Sterility assurance), Quality Assurance, Engineering / Validation,
Contract Manufacturing
Contract Development & Manufacturing Organisations (CMO & CDMO) Rapid validation for bio-decontamination. Enzyme Indicators offer benefits in the following core pharmaceutical disciplines such as Technical
Original Equipment Manufacturers
Enzyme Indicator Technology in Equipment Design Enzyme Indicators offer significant advantages for manufacturers of complex, often bespoke equipment for filling lines and production facilities for
Engineering
(Pharmaceutical Facilities Design)
Enzyme Indicator Technology Enzyme Indicators offer significant advantages when designing and building pharmaceutical manufacturing facilities. Protak work in partnership with contract validation and testing consultants
Hospital Pharmacy & Compounding
Safety and Quality Safety and quality concerns of medications are increasingly seeing healthcare providers opting to bring drug compounding under their own control. Protak work
Universities and Research Organisations
Biosafety Research laboratories and Cleanrooms processing pathogenic materials, such as those where medical conditions and illnesses are researched as well as animal research facilities –
Process Validation
Our validation process delivers quantifiable results in seconds, compared to the traditional validation tool with a 7 day incubation period, generating ‘challenge area’ specific data reducing cost, saving time and improving efficiency.
Our team will first understand your challenges then give a detailed presentation of our technology, equipment and capabilities while establishing the most effective usage of Enzyme Indicators for your bio-decontamination processes.
Meet us
View our calender to find out the full list of events we will be attending.
