Aztec Medical
Aztec Medical have been offering regulatory, design assurance and clinical consulting services to the medical device industry for over 20 years. Offering both remote and on-site support, we ensure th...
Aztec Medical's Basic Information
Industry
Medical Equipment Manufacturing
Headquarters
Gaillimh, Connaught, Ireland
Website
Headcount
2 - 10
Specialties
Strategic Regulatory AffairsRegulatory Approvals and Global Device RegistrationsMDR in EuropePost Approval ActivitiesTechnical WritingDesign AssuranceRisk ManagementClinical Evaluation ReportsClinical DocumentationEFS Study Approval: FDAIDE ApprovalClinical Investigation BrochuresVigilance and MDR ReportingCompetent Authority and Ethics ApprovalsCE Marking510(k) ClearancePMA ApprovalAustralia Clinical ApprovalsInterpretation of StandardsMeddev 2.7.1 Rev 4
Aztec Medical's Competitors
Vitalcor, Inc.
Westmont, California, United States
SteriPack Contract Manufacturing Laboratory
Poland
HealthCare Options, Inc.
Boca Raton, Florida, United States
Voxello
Coralville, Iowa, United States
OMEGA SITE ENGINEERING LTD
Haverhill, Florida, United States
Employee Insights
Employee Function
Employee Location
Aztec Medical's Top Employees
Dulce Zavala
Director DE Marketing Digital
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Frequently Asked Questions Regarding Aztec Medical
Where is Aztec Medical's headquarter located?
Aztec Medical's headquarter are located at Ireland.
How many employees does Aztec Medical have?
Aztec Medical has 2 - 10 employees.
What is Aztec Medical's official website?
Aztec Medical's official website is http://aztecmedical.com
What industry does Aztec Medical belong to?
Aztec Medical is in the industry of Medical Equipment Manufacturing
What does Aztec Medical do?
Aztec Medical have been offering regulatory, design assurance and clinical consulting services to the medical device industry for over 20 years. Offering both remote and on-site support, we ensure th...
What specialty does Aztec Medical have?
Strategic Regulatory AffairsRegulatory Approvals and Global Device RegistrationsMDR in EuropePost Approval ActivitiesTechnical WritingDesign AssuranceRisk ManagementClinical Evaluation ReportsClinical DocumentationEFS Study Approval: FDAIDE ApprovalClinical Investigation BrochuresVigilance and MDR ReportingCompetent Authority and Ethics ApprovalsCE Marking510(k) ClearancePMA ApprovalAustralia Clinical ApprovalsInterpretation of StandardsMeddev 2.7.1 Rev 4
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