Digitizing validation

We enable regulated organizations to move from paper-based validation to intelligent, digitized, paperless solutions.

And we do it through the ongoing development of a powerful, purpose-built software platform. In 2014, after 8 years of intensive software development, we launched the world’s most advanced validation software to help revolutionize the speed, precision, transparency and intelligence of validation in the Life Sciences sector. The solution is now used by some of the world’s leading Life Sciences companies.

Our new implementations range from a single validation process, in one location, to full deployments for multiple processes over many sites, with thousands of users; all supported by our teams in the US, Ireland and Switzerland. Our global operational headquarters and development teams are based in Ireland, and the company is listed on the Canadian Stock Exchange (TSX-V: KSI).

Bringing speed, intelligence, quality and compliance to where there was inefficiency, error and frustration

Helping life sciences move to end-to-end paperless validation was going to require the development of a very comprehensive, intelligent software platform. There were some basic software solutions available but nothing that could deliver a home-run. From day one we set out to create the ‘best-in-class’ solution. One that could 100% enable digitization and instigate a mass movement from the world of clunky paper-based validation. We were fortunate to assemble an outstanding development team in Ireland and to receive excellent advisory and financial support from our investment partners.

In 2014 the first, fully complete, fully tested model rolled out. It was an instant hit, is now used by some of the world’s leading life sciences companies and is quickly gaining acceptance as the top solution for the digital transformation of all commissioning, qualification and validation processes. It’s very satisfying to bring speed, intelligence, quality and compliance to an industry where there was inefficiency, error and frustration.

- Eddie Ryan, CEO, Kneat

Our Journey

2007
An expert team is formed

After concept evaluation coding began in earnest, an expert team is then formed comprising some of Ireland’s most brilliant software developers and pharma experts. By 2008 interest in Kneat had grown, as Irish Government Innovation funding is secured.

2009-2014
Development intensifies

Iterative development results in many prototypes and beta releases. By 2014 over 900,000 lines of cutting-edge code is written, with Kneat becoming ISO 9001 certified. Kneat’s first customers begin deployment in late 2014, following eight years of development in total.

2016-2018
Strong growth 

Following the completion of a reverse takeover resulting in a public listing and large capital injection, in 2016 the first of many Tier One Biopharma companies completes deployment of Kneat globally. The following year, in an industry world first, a Tier One Biotech company uses Kneat to manage all facilities, utilities and equipment C&Q activities for a new 1 Billion USD plant construction. EU and US Sales Directors are appointed to support demand in European, US and Asian markets.

Team

Extensive industry experience matched with exceptional technical capability

Directors

Eddie Ryan

CEO, Co-Founder

Brian Ahearne

Quality Director, Co-Founder

Kevin Fitzgerald

R&D Director, Co-Founder

Sarah Oliver

CFO

Non-executive Directors

Ian Ainsworth

Chairman

Paul Breen

Director

Wade Dawe

Director

Memberships & Accreditations

Event

Meet us at KenX Dublin 2018

We’re attending and exhibiting at the 2018 Computer Systems Validation & Data Integrity Compliance Congress in Dublin, Ireland on November 19th to 21st; meet us there for a full product demonstration.

Venue: Spencer Hotel
Location: Dublin, Ireland
Dates: 19-21 November 2018

Contact

Talk to us

Find out how Kneat can make your validation easier, faster, and smarter.
Start your validation revolution by speaking to our experts.

Europe: +353-61-203826
USA: (813)-503-6654
Canada: 1-902-442-7185