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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Jobs near you
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Manager of FDA and EMA Regulatory Affairs - IND Specialist - US East Coast Based Role
Merito Group
1 week agoVienna us
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
4.5 (25)
Practical Regulatory Affairs 2020 - European Medical Devices
A practical course discussing the EU Medical Device Regulation (MDR) in real-world situations
4.4 (266)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.
4.6 (10)Regulatory Affairs & Medical Writing
Expand your opportunities and CV
4.3 (24)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
4.1 (165)Global Pharma Regulatory Affairs course
Global Regulatory Affairs
3.2 (52)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
4.4 (7)European Medical Device Regulatory Basics
A beginner's primer to medical device regulation in Europe.
4.4 (28)US Regulatory Strategy for Biologics & Pharmaceutical Drugs
Learn how to navigate the US FDA regulations for getting your drug from bench to bedside.
4.2 (79)Drug Regulatory Pathways, Data and Market Exclusivity US AU
Rx and OTC Medicinal Products
4.4 (4)Quality and Regulatory: EU Product Legislation & CE Marking
Manufacturing, importing, selling and marketing products in Europe: obligations, responsibilities and liabilities.
3.7 (79)Regulatory Examination RE5 Test Preparation
RE5 Test Preparation for Representatives
3.2 (13)Legal and Regulatory aspects of Registration of Charges
A-Z guide of Charges under Indian Companies Act 2013
5.0 (2)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.
4.0 (12)Registration of Medical Devices for Sale in Singapore
The Singapore Regulatory and Registration Procedures for the Sale of Medical Devices
4.3 (9)eCTD & CTD Preparation & Submission Course
Pharmaceutical eCTD & CTD Preparation & Submission
3.7 (3)[2021] MEDICAL DEVICE: TEST METHOD VALIDATION
Master Test Method Validation Techniques in Healthcare Industry
3.7 (48)Applied ISO14971 Medical Device Risk Management
A concise guide to executing ISO 14971 requirements
4.3 (305)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
3.7 (181)Medical Device Development
A basic level primer for those starting their careers developing medical devices in a heavily regulated environment.
4.4 (67)