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FDA Presubmission Program – Requesting FDA Feedback
NSF International, Health Sciences
|
Professional Training
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From 299 USD
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Online
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Self-Paced Online
The Q-Sub program is a voluntary mechanism to get FDA’s feedback on specific questions necessary to guide product development and/or...
Clinical Investigations and Post Market Clinical Studies - Online Academy
PTI
|
Professional Training
5.0
(1)
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From 690 GBP
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Online
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Self-Paced Online
To improve patient safety the Medical Device Regulation (MDR) puts a greater emphasis on clinical data to provide evidence of...
Fundamentals of EU Regulatory Affairs
PTI
|
Professional Training
5.0
(2)
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From 950 GBP
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Online
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Self-Paced Online
The pharmaceutical and biotech industries are the most regulated in the world due to the nature of the product. Patient...
Quality Improvement Science and Systems Analysis
University of Oxford
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Short University Courses
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This course results in CPD hours
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Oxford
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Classroom
The Quality Improvement Science and Systems Analysis course introduces the principles and core methodology of industrial quality improvement methods with...
Essentials of In-Vitro Diagnostics Regulatory Affairs
The Organisation for Professionals in Regulatory Affairs
|
Professional Training
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From 360 GBP
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Online
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Self-Paced Online
This course will provide a basic awareness of the regulatory environment and an appreciation of some of the main regulatory...
Quality & Quality Improvement in Healthcare
University of Leicester
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Short University Courses
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Leicester
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Classroom
Course Outline In this course you will investigate major approaches to quality in healthcare, with a particular emphasis on approaches...
Supervisory Skills for Technical Services
University of Leeds - Faculty of Engineering and Physical Sciences
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Professional Training
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This course results in CPD hours
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Leeds
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Classroom
Good supervision of aseptic processing is essential for ensuring a high quality, efficient and safe service. As the quality of...
FDA Inspection Readiness Training
NSF International, Health Sciences
|
Professional Training
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Beginner level
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From 1,200 USD
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Online
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Virtual Classroom
Understanding what to expect during an FDA inspection enables a medical device manufacturer to prepare effectively for an FDA inspection....
ISO 45001:2018 Introduction
Intu Veritas Ltd
|
Professional Training
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Nationwide
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In Company
For individuals and organisations seeking an understanding of ISO 45001:2018 and it’s requirements including Annex SL and the High Level...
A Practical Guide to Pharmacovigilance
PTI
|
Professional Training
5.0
(3)
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From 999 GBP
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Online
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Self-Paced Online
Through this online course participants will develop their knowledge of key regulations and guidelines relating to PV - and how...
Biopharma Due Diligence Evaluations
PTI
|
Professional Training
5.0
(2)
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From 330 GBP
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Online
-
Self-Paced Online
Due diligence evaluations are a critical and often challenging part of the deal making process as detailed analysis is conducted...
Design Controls for Medical Devices
NSF International, Health Sciences
|
Professional Training
4.5
(2)
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Intermediate level
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From 1,200 USD
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Online
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Virtual Classroom
This course provides an understanding of design control principles and the design and development regulatory requirements relative to U.S. 21...
Post-Market Surveillance and Vigilance for Medical Devices
The Organisation for Professionals in Regulatory Affairs
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Professional Training
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From 1,700 GBP
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Multiple (2)
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Classroom, Self-Paced Online
This Masterclass is also Module 16 of the MSc Regulatory Affairs and will help to define the terminology and explain...
Effects of Radiation: An Introduction to Radiation and Radioactivity
edX
|
Professional Training
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Beginner level
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Online
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Self-Paced Online
There are many practical applications of radiation and radioactivity in various fields, including medical, scientific, and industrial activities. In some...
Medical Device Regulatory Project Management
PTI
|
Professional Training
-
From 1,595 GBP
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London
-
Classroom
How can regulatory affairs professionals benefit from project management in the medical devices industry? 2020 marks an important date for...
Medical Device Regulatory Project Management
PTI
|
Apprenticeship training for companies
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From 1,595 GBP
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Multiple (2)
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Classroom, Self-Paced Online
How can regulatory affairs professionals benefit from project management in the medical devices industry? 2020 marks an important date for...
Advanced EU Regulatory Affairs
PTI
|
Professional Training
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From 1,400 GBP
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Online
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Virtual Classroom
Being a regulatory affairs professional in a pharmaceutical or biotech company is both challenging and rewarding. As a senior professional...
Advanced European Regulatory Affairs
PTI
|
Professional Training
5.0
(1)
-
This course results in CPD hours
-
From 1,995 GBP
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London
-
Classroom
Being a regulatory affairs professional in a pharmaceutical or biotech company is both challenging and rewarding. As a senior professional you must ensure...
Essentials of European Pharmaceutical Regulatory Affairs
The Organisation for Professionals in Regulatory Affairs
|
Professional Training
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From 580 GBP
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Online
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Self-Paced Online
This course will provide a basic, comprehensive grounding in pharmaceuticalregulatory affairs in a relaxed and interactive environment. This popular course...
Essentials of European Regulatory Affairs (Online Course)
The Organisation for Professionals in Regulatory Affairs
|
Professional Training
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From 340 GBP
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Online
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Self-Paced Online
The world of Regulatory Affairs can be a confusing and complex place, particularly if you have no formal industry background....
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