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Regulatory Affairs Specialist Skills in Scientific

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Top Regulatory Affairs Specialist skills in Scientific

Below we've put together a list of the skills needed for Regulatory Affairs Specialist. We ranked the top skills based on the percentage of Regulatory Affairs Specialist job descriptions they appeared on. For example, 21% of Regulatory Affairs Specialist job descriptions contained Regulatory Affairs as a skill.

The most common skills found on Regulatory Affairs Specialist job descriptions in 2021.

Keywords Popularity
Regulatory Affairs
21%
Medical Devices
14%

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Online Courses for Regulatory Affairs Specialist

One of the best ways to acquire the skills for a role is to take an online course. We've identified some online courses from Udemy that will help you advance in your career.

Practical Regulatory Affairs 2020 - US FDA Medical Devices

A practical course discussing the US FDA Medical Device regulations for real-world situations

Udemy logo 4.5 (25)
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Practical Regulatory Affairs 2020 - European Medical Devices

A practical course discussing the EU Medical Device Regulation (MDR) in real-world situations

Udemy logo 4.4 (266)
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Medical Device Regulation 2017/745 EU regulatory affairs.

Understand the European MDR 2017/745 in simple terms to gain market approval of a medical device in the EU.

Udemy logo 4.6 (10)
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Regulatory Affairs & Medical Writing

Expand your opportunities and CV

Udemy logo 4.3 (24)
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EU Medical Device Regulatory Affairs explained Simply

How to get approval to sell your Medical Devices within the European Union. Rules explained in simple format for student

Udemy logo 4.1 (165)
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Global Pharma Regulatory Affairs course

Global Regulatory Affairs

Udemy logo 3.2 (52)
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EU MDR Regulation 2017/745 - Essential Awareness Exam

Self Assess and improve your knowledge on the essentials of EU MDR 2017/745 which is going to be enforced on May-2020

Udemy logo 4.4 (7)
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European Medical Device Regulatory Basics

A beginner's primer to medical device regulation in Europe.

Udemy logo 4.4 (28)
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US Regulatory Strategy for Biologics & Pharmaceutical Drugs

Learn how to navigate the US FDA regulations for getting your drug from bench to bedside.

Udemy logo 4.2 (79)
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Drug Regulatory Pathways, Data and Market Exclusivity US AU

Rx and OTC Medicinal Products

Udemy logo 4.4 (4)
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Quality and Regulatory: EU Product Legislation & CE Marking

Manufacturing, importing, selling and marketing products in Europe: obligations, responsibilities and liabilities.

Udemy logo 3.7 (79)
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Regulatory Examination RE5 Test Preparation

RE5 Test Preparation for Representatives

Udemy logo 3.2 (13)
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Legal and Regulatory aspects of Registration of Charges

A-Z guide of Charges under Indian Companies Act 2013

Udemy logo 5.0 (2)
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21 CFR Part 820 (Medical Device QSR) - Practice Exam

21 CFR Part 820 Exam - Self Assessment Exam to validate your QSR knowledge, Medical Devices Regulatory Framework etc.

Udemy logo 4.0 (12)
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Registration of Medical Devices for Sale in Singapore

The Singapore Regulatory and Registration Procedures for the Sale of Medical Devices

Udemy logo 4.3 (9)
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eCTD & CTD Preparation & Submission Course

Pharmaceutical eCTD & CTD Preparation & Submission

Udemy logo 3.7 (3)
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[2021] MEDICAL DEVICE: TEST METHOD VALIDATION

Master Test Method Validation Techniques in Healthcare Industry

Udemy logo 3.7 (48)
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Applied ISO14971 Medical Device Risk Management

A concise guide to executing ISO 14971 requirements

Udemy logo 4.3 (305)
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ISO 13485:2016 - Design and Development of Medical Devices

Design and Development of Medical Devices in the perspective of ISO 13485:2016 and Medical Devices Industry

Udemy logo 3.7 (181)
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Medical Device Development

A basic level primer for those starting their careers developing medical devices in a heavily regulated environment.

Udemy logo 4.4 (67)
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