Solidsoft Reply Limited
Budget
€10 — €0
EP Access
0
accredited persons
Staff
3
0.45 FTE
EU Grants
None
Mission & Goals
Solidsoft Reply is a technology company working in the healthcare and pharmaceutical sectors. We built and run the European Medicines Verification System used to verify approximately ten billion packs of medicine across the EU each year at 160,000 points of dispense. We operate national medicine verification systems in 14 EU countries. We build verification and traceability systems used across the world, together with healthcare-related systems focused on patient and medicine safety. We work with non-profit organisations (UNICEF, USAID, GAVI, etc.), NGOs and the pharmaceutical industry combatting falsified and counterfeit medicines and reducing vaccine hesitancy in low- and middle-income countries. Based in the UK, we are part of the Reply Group of technology companies headquartered in Milan in Italy. Reply operates across the EU and other regions of the world.
EU Legislative Interests
Much of our work centres on two pieces of existing EU legislation: Directive 2011/62/EU amending Directive 2001/83/EC. This is commonly known as the Falsified Medicines Directive (FMD) Commission Delegated Regulation (EU) 2016/161 supplementing the FMD. The EU is currently engaged in a major review of Directive 2001/83/EC with a view to introducing new and updated legislation which we expect to affect our work in medicines verification and traceability. To date, our main communication with the EU is via the European Medicines Verification Organization (EMVO), a stakeholder non-profit organisation mandated by EU law and headquartered in Brussels. Going forward, we are currently planning to support and participate in the European Critical Medicines Alliance announced by the Health Emergency Preparedness and Response Authority (HERA) with a specific interest in addressing medicine shortages across the Union.
Communication Activities
In addition to our Web Site, we contribute regularly to thought leadership and discussion via Linked-In and attend various pharmaceutical events with a focus on medicine safety and verification.
Interests Represented
Promotes their own interests or the collective interests of their members
Member Of
GS1 Partner https://www.gs1uk.org/partner-finder
Connected Legislation
Commissioner Meetings
No recorded meetings with EU commissioners.