Certificate in Medical Devices Directive, CE Marking for Europe (93/42/EEC)

OR

Medical Devices Directive course after Pharmacy

Prepared by Docthub Courses Team ∣

Last updated on 03 Feb 2025

Overview

The Certificate in Medical Devices Directive, CE Marking for Europe (93/42/EEC) is a specialized course focused on regulatory compliance for medical devices. It belongs to the field of regulatory affairs and medical device management. The course typically spans a few weeks to a couple of months, depending on the provider. It covers the essential aspects of the EU Medical Devices Directive.

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Institute of Good Manufacturing Practices (IGMPI), New Delhi

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Delhi

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New Delhi

Related Job Roles

Medical Device Engineer

Medical Equipment Specialist

Biomedical Equipment Technician

Medical Device Sales Representative

Medical Device Development Specialist

Medical Device Risk Management Specialist

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Certificate in Medical Devices Directive, CE Marking for Europe (93/42/EEC)

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Qualifications

BTech Biomedical Engineering

Diploma in Bio Medical Waste Management

Related Specialty

Medical Devices

Pathology Equipment Engineering

Radiology Equipment Engineering

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