About Reassurance.ie

We are offering a digital technology platform combined with a multilayered testing system which will detect Covid 19 Infectiousness in an immediate and progressive manner and thereby facilitate a safe resumption of all economic, social and educational activities.

We are an Irish business which has established testing centres to help detect and reduce the spread of COVID 19. The business was set up by three pharmacists, Chris O’Grady, James Cloney and Aidan Kelly of Duelchem Ltd, a long-established supplier of pharmaceutical products to the Irish healthcare sector.

Reassurance.ie has access to significant supplies of both PCR and Antigen tests, all of which are EU approved and carry the CE mark. We have highly skilled staff who are trained to administer and supervise these tests. Our objective is to get Ireland back to normal living in a safe way while always adhering to best medical practice. Reassurance.ie have partnered with an international digital platform to underpin our testing programme. The testing programme and the platform are highly adaptable and can be customised for any workplace, event or venue.

By combining a multi-layered testing programme with a digital health platform, reassurance.ie and tested.me aims to enable individuals to return to a more normal life of work, travel, education, sport and culture as safely and as quickly as possible. We are located in Dublin and Kilkenny, with both national and international coverage.

About Duelchem Limited

Duelchem Limited is an Irish company that was set up in 2008, regulated by the HPRA.
We have been supplying the Irish Health Care sector with pharma products for over a decade.

We supply medicinal products including Controlled Drugs (CD’s), Parallel Imports (PI’s) and Exempt Medicinal Products (EMP’s). We also supply medicinal devices, medicinal/laboratory consumables and equipment. We are registered with the ‘Irish Medicines Verification Organisation (IMVO)’ (account no. IMVO-EU-1403) and are fully compliant with the ‘Falsified Medicine Directive (FMD)’.

As part of our HPRA obligations, our regulatory affairs team ensure we are prepared for and comply with legislative changes such as the ‘Medicinal Devices Regulation (MDR)’ and ‘In-Vitro Diagnostic Devices Regulation (IVDR)’.