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Quick Pharm Solutions

Quick Pharm Solutions provide software & hardware solutions across all countries for the Falsified Medicines Directive (FMD) and Medical Devices Regulation (MDR).


Quick Pharm Solutions is a GS1 Ireland Solution Partner 2024.

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View the Quick Pharm Solutions Listing on the GS1 Solution Provider Directory

Connecting you to your National Medicines Verification System ("NMVS") to meet EU Falsified Medicines Directive requirements.

Quick Pharm Solutions have developed an out of the box solution called EasyFMD that will allow you to meet your obligations under the European Falsified Medicines directive which came into effect in February 2019. EasyFMD has been specifically developed for pharmaceutical wholesalers, hospitals and retail pharmacies and is capable of high volume scanning. EasyFMD works in conjunction with our versatile compact high speed conveyor scanning solution which is also compatible with hand held scanner functionality.

Pharmacies, Hospitals and Wholesalers

If you are a retail pharmacy, a hospital, a wholesaler or any other healthcare institution that needs to connect to your National Medicines Verification System ("NMVS") to fulfil your obligations arising from the EU Falsified Medicines Directive, then our EasyFMD solution provides all the necessary functionality to allow you to become FMD compliant quickly and easily and with minimum impact on staff and budgets. For a complete list of EasyFMD features and benefits, please click here.

Manufacturers and Parallel Importers

If you are a manufacturer or parallel importer that needs to connect directly to EMVO to upload product and pack data, then we can help you initially with the entire onboarding process. Once onboarding is complete, our Direct Connect Manager solution provides all the necessary functionality to allow you to complete all the steps required to upload your product master data, serialise packs and then upload the serialised pack data to EMVO.

For a complete list of Direct Connect Manager features and benefits, please click here.

Medical Devices Regulation

MDR software for Wholesalers, Importers, Hospitals and Health Care Institutions to meet their compliance obligations under the European Commission Medical Devices Regulations (2017/745/EU) (MDR) and (2017/746/EU) (IVDR). EudaMed Connect, our MDR Software Solution, is designed to allow you meet your compliance obligations under the European Commission Medical Devices Regulation (MDR). If you are a pharmaceutical wholesaler, importer, hospital or health care institution then the Medical Devices Regulation (2017/745/ EU) (MDR) and (2017/746/EU) (IVDR) could be applicable to you. The Class III Medical Devices EU regulation and obligations came into effect on 26 May 2021 and a staggered period is in place until 2025. EudaMed Connect provides the ability to scan incoming serialised Medical Devices that includes a UDI (Unique Device Identifier) and provide additional device information when connected to the EU EudaMed database.

 For a complete list of EudaMed Connect features and benefits, please click here

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