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.
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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.
A practical course discussing the US FDA Medical Device regulations for real-world situations4.5 (25)
A practical course discussing the EU Medical Device Regulation (MDR) in real-world situations4.4 (266)
Understand the European MDR 2017/745 in simple terms to gain market approval of a medical device in the EU.4.6 (10)
Expand your opportunities and CV4.3 (24)
How to get approval to sell your Medical Devices within the European Union. Rules explained in simple format for student4.1 (165)
Global Regulatory Affairs3.2 (52)
Self Assess and improve your knowledge on the essentials of EU MDR 2017/745 which is going to be enforced on May-20204.4 (7)
A beginner's primer to medical device regulation in Europe.4.4 (28)
Learn how to navigate the US FDA regulations for getting your drug from bench to bedside.4.2 (79)
Rx and OTC Medicinal Products4.4 (4)
Manufacturing, importing, selling and marketing products in Europe: obligations, responsibilities and liabilities.3.7 (79)
RE5 Test Preparation for Representatives3.2 (13)
A-Z guide of Charges under Indian Companies Act 20135.0 (2)
21 CFR Part 820 Exam - Self Assessment Exam to validate your QSR knowledge, Medical Devices Regulatory Framework etc.4.0 (12)
The Singapore Regulatory and Registration Procedures for the Sale of Medical Devices4.3 (9)
Pharmaceutical eCTD & CTD Preparation & Submission3.7 (3)
Master Test Method Validation Techniques in Healthcare Industry3.7 (48)
A concise guide to executing ISO 14971 requirements4.3 (305)
Design and Development of Medical Devices in the perspective of ISO 13485:2016 and Medical Devices Industry3.7 (181)
A basic level primer for those starting their careers developing medical devices in a heavily regulated environment.4.4 (67)