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Practical Requirements of the Arab Pharmacovigilance Guidelines
4.8
(4)
International Professional & Industry Academy
On 1 July 2015, the Common Arab Guidelines on good vigilance practices became effective. The Guidelines represented fundamental changes to...
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Professional Training
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2 days
-
From 1,099 GBP
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Online
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Virtual Classroom
FDA Presubmission Program – Requesting FDA Feedback
NSF International, Health Sciences
The Q-Sub program is a voluntary mechanism to get FDA’s feedback on specific questions necessary to guide product development and/or...
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Professional Training
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2 hours
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From 299 USD
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Online
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Self-Paced Online
An Essential Overview of Pharmacovigilance
4.7
(18)
International Professional & Industry Academy
Pharmacovigilance has undergone rapid regulatory change in recent years and become one of the most demanding aspects of the pharmaceutical...
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Professional Training
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From 549 GBP
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Online
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Virtual Classroom
Pharmacovigilance
4.4
(32)
International Professional & Industry Academy
This comprehensive three-day pharmacovigilance training course has been designed to provide an introductory guide for all those concerned with vigilance...
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Professional Training
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3 days
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Multiple (2)
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Virtual Classroom, Classroom
Clinical Investigations and Post Market Clinical Studies - Online Academy
5.0
(1)
PTI
To improve patient safety the Medical Device Regulation (MDR) puts a greater emphasis on clinical data to provide evidence of...
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Professional Training
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4 weeks
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From 690 GBP
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Online
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Self-Paced Online
Fundamentals of EU Regulatory Affairs
5.0
(2)
PTI
The pharmaceutical and biotech industries are the most regulated in the world due to the nature of the product. Patient...
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Professional Training
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4 weeks
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From 950 GBP
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Online
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Self-Paced Online
Quality Improvement Science and Systems Analysis
University of Oxford
The Quality Improvement Science and Systems Analysis course introduces the principles and core methodology of industrial quality improvement methods with...
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Short University Courses
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Oxford
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Classroom
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This course results in CPD hours
Essentials of In-Vitro Diagnostics Regulatory Affairs
The Organisation for Professionals in Regulatory Affairs
This course will provide a basic awareness of the regulatory environment and an appreciation of some of the main regulatory...
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Professional Training
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1 day
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From 360 GBP
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Online
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Self-Paced Online
Quality & Quality Improvement in Healthcare
University of Leicester
Course Outline In this course you will investigate major approaches to quality in healthcare, with a particular emphasis on approaches...
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Short University Courses
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Leicester
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Classroom
Understanding Pharmacovigilance Regulations in APAC
International Professional & Industry Academy
Pharmacovigilance regulations in Asia are dynamic and fast-changing. As the Asia-Pacific region becomes increasingly important for pharmaceutical companies, it's vital...
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Professional Training
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From 549 GBP
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Online
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Virtual Classroom
EU Pharmaceutical Regulations & Strategy
4.2
(17)
International Professional & Industry Academy
Creating and coordinating an effective regulatory strategy is an essential part of the work of a regulatory affairs department and...
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Professional Training
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2 days
-
From 1,099 GBP
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Online
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Virtual Classroom
Regulatory Affairs for Support Staff
4.4
(18)
International Professional & Industry Academy
Working in pharmaceutical regulatory affairs is a challenging role, with involvement in the drug development stages, the marketing authorisation submission...
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Professional Training
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2 days
-
From 1,099 GBP
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Online
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Virtual Classroom
Supervisory Skills for Technical Services
University of Leeds - Faculty of Engineering and Physical Sciences
Good supervision of aseptic processing is essential for ensuring a high quality, efficient and safe service. As the quality of...
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Professional Training
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1 day
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Leeds
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Classroom
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This course results in CPD hours
ISO 45001:2018 Introduction
Intu Veritas Ltd
For individuals and organisations seeking an understanding of ISO 45001:2018 and it’s requirements including Annex SL and the High Level...
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Professional Training
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1 day
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Nationwide
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In Company
FDA Inspection Readiness Training
NSF International, Health Sciences
Understanding what to expect during an FDA inspection enables a medical device manufacturer to prepare effectively for an FDA inspection....
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Professional Training
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2 days
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From 1,200 USD
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Online
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Virtual Classroom
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Beginner level
Design Controls for Medical Devices
4.5
(2)
NSF International, Health Sciences
This course provides an understanding of design control principles and the design and development regulatory requirements relative to U.S. 21...
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Professional Training
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2 days
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From 1,200 USD
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Online
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Virtual Classroom
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Intermediate level
A Practical Guide to Pharmacovigilance
5.0
(3)
PTI
Through this online course participants will develop their knowledge of key regulations and guidelines relating to PV - and how...
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Professional Training
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From 999 GBP
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Online
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Self-Paced Online
Biopharma Due Diligence Evaluations
5.0
(2)
PTI
Due diligence evaluations are a critical and often challenging part of the deal making process as detailed analysis is conducted...
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Professional Training
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3 weeks
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From 330 GBP
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Online
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Self-Paced Online
Post-Market Surveillance and Vigilance for Medical Devices
The Organisation for Professionals in Regulatory Affairs
This Masterclass is also Module 16 of the MSc Regulatory Affairs and will help to define the terminology and explain...
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Professional Training
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3 days
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From 1,700 GBP
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Multiple (2)
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Classroom, Self-Paced Online
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