Med-Di-Dia Limited
Med-Di-Dia, a regulatory affairs and quality compliance consultancy focusing on the Medical, Digital Health and Diagnostic sectors of the European Life Science Industry. With passion and drive we hav...
Med-Di-Dia Limited's Basic Information
Industry
Medical Equipment Manufacturing
Headquarters
Gaillimh, Connaught, Ireland
Website
Founded Year
2018
Headcount
2 - 10
Specialties
Regulatory AffairsQuality ComplianceMedical DevicesDigital HealthDiagnosticsEU Authorised RepresentativeEU Person ResponsibleEU Legal RepresentativeTechnical FilesRegulatory StrategyClinical InvestigationsClinical EvaluationsDesign FilesDesign ControlSoftware ValidationRisk ManagementISO 13485Quality Management SystemsCorrective and Preventive Action (CAPA)Product ClassificationNotified BodiesEUARMedTech DeviceQuality Management
Med-Di-Dia Limited's Competitors
PureWay Compliance
Santa Monica, California, United States
Medicare Uitgeest BV
Netherlands
Medical Devices Alliance
Medex Loncin
Belgium
Banyan Stat Kits
Mukilteo, Washington, United States
Employee Insights
Employee Function
Employee Location
Med-Di-Dia Limited's Top Employees
Bobby Deal
Owner-Managing Director
Greer Deal
Director
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Frequently Asked Questions Regarding Med-Di-Dia Limited
Where is Med-Di-Dia Limited's headquarter located?
Med-Di-Dia Limited's headquarter are located at Ireland.
How many employees does Med-Di-Dia Limited have?
Med-Di-Dia Limited has 2 - 10 employees.
What is Med-Di-Dia Limited's official website?
Med-Di-Dia Limited's official website is http://med-di-dia.com
What industry does Med-Di-Dia Limited belong to?
Med-Di-Dia Limited is in the industry of Medical Equipment Manufacturing
What does Med-Di-Dia Limited do?
Med-Di-Dia, a regulatory affairs and quality compliance consultancy focusing on the Medical, Digital Health and Diagnostic sectors of the European Life Science Industry. With passion and drive we hav...
What specialty does Med-Di-Dia Limited have?
Regulatory AffairsQuality ComplianceMedical DevicesDigital HealthDiagnosticsEU Authorised RepresentativeEU Person ResponsibleEU Legal RepresentativeTechnical FilesRegulatory StrategyClinical InvestigationsClinical EvaluationsDesign FilesDesign ControlSoftware ValidationRisk ManagementISO 13485Quality Management SystemsCorrective and Preventive Action (CAPA)Product ClassificationNotified BodiesEUARMedTech DeviceQuality Management
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