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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
Advanced Regulatory Affairs for Medical Devices
4.1
(8)
International Professional & Industry Academy
The regulatory environment for medical devices is in a transitional period. With the increased focus on patient safety, the MDR...
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Professional Training
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From 1,099 GBP
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Online
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Virtual Classroom
Advanced Regulatory Affairs for Medical Devices
4.6
(5)
PTI
The Medical Devices Regulation (MDR) was concluded in June 2016, which means significant changes for the European regulatory landscape for medical...
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Professional Training
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2 days
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From 1,595 GBP
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Multiple (3)
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Classroom
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This course results in CPD hours
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Advanced level
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices
International Professional & Industry Academy
The ISO 13485:2016 standard specifies requirements for a Quality Management System (QMS) where an organisation needs to demonstrate its ability...
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Professional Training
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1 day
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From 549 GBP
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Online
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Virtual Classroom
Essentials of European Medical Device Regulatory Affairs
The Organisation for Professionals in Regulatory Affairs
This course provides an opportunity that on-the-job learning doesn't: network and learn from a variety of experts including your fellow...
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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
FDA Approval Process for Medical Devices
4.6
(29)
International Professional & Industry Academy
This seminar will provide a solid foundation in the approval and clearance processes for medical devices in the United States....
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Professional Training
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2 days
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From 1,099 GBP
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Multiple (2)
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Virtual Classroom, Classroom
Fundamentals of EU Regulations for Medical Devices
PTI
Are you ready for the new Medical Device Regulation (MDR)? Published on May 5th 2017, the final text of the...
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Professional Training
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5 weeks
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From 999 GBP
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Online
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Self-Paced Online
Introduction to Regulatory Affairs for Medical Devices
5.0
(5)
PTI
Following its ratification by the European Parliament, the Medical Devices Regulation will constitute major changes for the industry and is...
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Professional Training
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2 days
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From 1,595 GBP
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Multiple (3)
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Classroom
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This course results in CPD hours
Medical Device Regulation in the Eurasian Union, Russia and the CIS
4.2
(4)
International Professional & Industry Academy
The aim of this event is to provide a comprehensive overview of medical device regulatory affairs in Russia and the...
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Professional Training
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2 days
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From 1,099 GBP
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Online
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Virtual Classroom
Medical Device Regulations in the MENA Region
PTI
As healthcare spending continues to rise in the Middle East and North Africa (MENA), this region is becoming a key...
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Professional Training
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4 weeks
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Online
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Self-Paced Online
Medical Device Regulations in the Middle East and North Africa
4.5
(17)
International Professional & Industry Academy
The size of the medical device market in the Middle East has expanded over recent years and this trend is...
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Professional Training
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2 days
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From 1,099 GBP
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Online
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Virtual Classroom
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting
4.5
(22)
International Professional & Industry Academy
This seminar provides an essential overview of medical device clinical evaluations, clinical investigations and PMCF studies with particular emphasis on...
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Professional Training
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From 1,099 GBP
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Online
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Virtual Classroom
Medical Writing for Medical Devices
4.4
(12)
International Professional & Industry Academy
Writing for medical devices has its own particular skill set and, with important regulatory changes in the industry, all those...
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Professional Training
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2 days
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From 1,099 GBP
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Online
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Virtual Classroom
Post Market Surveillance and Vigilance Requirements for Manufacturers (EU 2017/745)
NSF International, Health Sciences
Post-market surveillance for manufacturers is covered in Articles 83-86. Articles 87-89 cover post-market vigilance requirements. This course reviews the requirements...
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Professional Training
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1 hour
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From 299 USD
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Online
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Self-Paced Online
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