Certificate in EU IVD Medical Device Regulation

OR

IVD Medical Device Regulation course after Pharmacy

Prepared by Docthub Courses Team ∣

Last updated on 03 Feb 2025

Overview

The Certificate in EU IVD Medical Device Regulation is a specialized course focused on European regulations for in vitro diagnostic medical devices. It typically spans a few weeks to a few months, depending on the provider. This course is part of the regulatory affairs and medical device industry fields. It covers key topics such as compliance requirements, regulatory pathways, and the latest EU directives affecting IVD devices. 

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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

Biomedical Engineer Manager

Medical Device Engineer

Validation Engineer

Diagnostic Imaging Technician

Biomedical Equipment Technician

Validation Specialist

Medical Device Development Specialist

Regulatory Affairs Product Manager

Medical Device Risk Management Specialist

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Related Course titles

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Certificate in EU IVD Medical Device Regulation

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Qualifications

MPharm Regulatory Affairs

MPharm (Master Of Pharmacy)

DPharm (Diploma in Pharmacy)

BTech Biomedical Engineering

Diploma in Biomedical Engineering

MTech Biomedical Engineering

BPharm (Bachelor Of Pharmacy)

Related Specialty

Medical Devices

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