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CE marking is compulsory for the greatest products protected by using the New Approach Directives.

AQC gives all knowledge regarding CE marking in medical devices consultancy.

CE MARK CERTIFICATION FOR MEDICAL DEVICE

WHAT IS CE MARKING? CE stands for Conformité Européenne, which translates from French to English as ‘European Conformity.CE Mark Certification indicates that a product has been assessed by the manufacturer and deemed to meet EU(European Union’s) safety health and environmental protection requirements.CE mark mandatory conformity marking for regulating the products sold within the European Economic

Alpine Quality Consultant provides Consulting services for Medical Device Industry. Our Team of Experts incorporates Healthcare Professionals, Regulatory Compliance Consultants, and Doctors. We give our service in small possible time and cost-effective way. MEDICAL DEVICE REGULATORY CONSULTING SERVICES Alpine Quality Consultants give direction and support to compliances by qualified, experienced, and executive Advisors and Experts

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