The organisation puts Patient Safety & Product Quality at the forefront of the business ethos working to the latest GMP & GDP regulations & guidelines overseen by the UK regulator the MHRA.
Dixons UK Ltd continue to verify through our EMVO approved product verification software. All EU imported POM product is verified upon receipt to confirm product status.
Qualified Person
Qualified Person
Utilising the latest risk based eQMS software to deliver industry best practice to manage compliance needs & meet current regulatory requirements allowing the team access to required modules for data entry, review & approval.
Monitoring the following areas of the business:
The eQMS comprises the following modules to aid in the delivery of our quality ethos:
As the quality team is independent an impartial approach is delivered directly to all departments during these inspections by utilising the Green and Orange guide to ensure all areas are compliant. These inspections are undertaken annually as a minimum or sooner if any area of concern is highlighted during the bi-annual PQR/MRM.
We undertake a risk-based approach and carry out dependant onsite & desktop inspections.
With the above in mind, all pharmaceutical suppliers and customers are fully qualified prior to trading and are fully re-qualified annually with additional bona-fide checks undertaken during the year.
DP UK Ltd only use temperature-controlled transport with fully licenced and certified 3PL providers who undergo the same stringent qualification procedure as customers and suppliers.
Need help with something? Get in touch with our friendly team.
Dixons Pharmaceuticals UK Ltd Unit F4 Ivanhoe Business Park, Tom Bill Way, Ashby de la Zouch Leicestershire, LE65 2UY
Dixons Pharmaceuticals CZ s.r.o
K Sokolovna 218,
Prague 10, Uhříněves
+44 (0) 1530 410920
+44 (0) 1530 410920
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