RQM+
RQM+ is the leading MedTech service provider with the world’s largest global team of regulatory and quality experts. Building upon 40 years of regulatory expertise, we also provide comprehensive clini...
RQM+'s Basic Information
Industry
Medical Equipment Manufacturing
Headquarters
Monroeville, Alabama, United States
Website
Founded Year
2008
Headcount
51 - 200
Specialties
Regulatory for Medical DeviceQuality Systems for Medical DeviceDesign Assurance for Medical DeviceProduct Quality for Medical DevicePost-Market Surveillance for Medical DeviceEU MDRClinical Evaluation ReportsRemediationForm 483, Warning Letter, Consent DecreeComplaint RemediationManufacturing Site Transfer510(k), PMA, De NovoUDI ComplianceSupplier QualityProcess ValidationHuman FactorsDesign Verification and ValidationDesign History File RemediationDesign Quality AssuranceFDA Mock AuditIn Vitro Diagnostics
RQM+'s Competitors
BD
Franklin Lakes, New Jersey, United States
DJO
Dallas, Georgia, United States
Isometric Micro Molding, Inc.
New Richmond, Ohio, United States
MD Diagnostics Ltd
Maidstone, England, United Kingdom
Uplift Technologies Inc
Employee Insights
Employee Function
Employee Location
RQM+'s Top Employees
DeVer Warner
Board of Directors
Richard Thomas
Director, Board Of Directors
Faisal Omar
Associate Engineer
Danny Oseid
Biocompatibility Associate – Toxicology Support
Joe Commane
Associate Engineer
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Frequently Asked Questions Regarding RQM+
Where is RQM+'s headquarter located?
RQM+'s headquarter are located at United States.
How many employees does RQM+ have?
RQM+ has 51 - 200 employees.
What is RQM+'s official website?
RQM+'s official website is https://www.rqmplus.com/
What industry does RQM+ belong to?
RQM+ is in the industry of Medical Equipment Manufacturing
What does RQM+ do?
RQM+ is the leading MedTech service provider with the world’s largest global team of regulatory and quality experts. Building upon 40 years of regulatory expertise, we also provide comprehensive clini...
What specialty does RQM+ have?
Regulatory for Medical DeviceQuality Systems for Medical DeviceDesign Assurance for Medical DeviceProduct Quality for Medical DevicePost-Market Surveillance for Medical DeviceEU MDRClinical Evaluation ReportsRemediationForm 483, Warning Letter, Consent DecreeComplaint RemediationManufacturing Site Transfer510(k), PMA, De NovoUDI ComplianceSupplier QualityProcess ValidationHuman FactorsDesign Verification and ValidationDesign History File RemediationDesign Quality AssuranceFDA Mock AuditIn Vitro Diagnostics
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