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ISO/IEC 17025 Competence of Testing & Calibration Laboratories Awareness
BSI Training
The general requirement for the testing and calibration laboratories is critically important to both you and your customers. That’s why...
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Professional Training
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From 65 GBP
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Multiple (2)
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Self-Paced Online, In Company
ISO 13485 Quality Management Systems — Requirements for Regulatory Purposes Awareness On-demand Training Course
BSI Training
Quality Management systems (QMS) in the medical device world is critically important to the safety of patients around the world....
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Professional Training
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From 65 GBP
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Multiple (2)
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Self-Paced Online, In Company
ISO 14971:2019 Risk Management: Requirements on-demand eLearning
BSI Training
This on-demand intensive course enables greater understanding of the impact that ISO 14971:2019 has on the decision-making process when manufacturing...
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Professional Training
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4 hours
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From 595 GBP
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Multiple (2)
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Self-Paced Online, In Company
ISO 13485:2016 Requirements On-demand eLearning
BSI Training
This training course explores the requirements of the ISO 13485:2016 Quality Management System standard, discussing key principles and how the...
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Professional Training
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4 hours
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From 495 GBP
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Multiple (2)
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Self-Paced Online, In Company
Implementation of IVDR for CE Marking On-demand eLearning course
BSI Training
The In Vitro Diagnostic Devices Regulation (IVDR 2017/746) is the legislation detailing the requirements which manufacturers have to meet to...
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Professional Training
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10 hours
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From 1,295 GBP
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Multiple (2)
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Self-Paced Online, In Company
The Future of Medicine
IIL Europe
This session focuses on the innovations in medicine and how this industry (much like humanity) is evolving. New technology in...
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Professional Training
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From 15 USD
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Online
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Self-Paced Online
Auditing QC Laboratories
NSF International, Health Sciences
This course provides you with the necessary skills and an understanding of how you can check for evidence of both...
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Professional Training
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2 days
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Multiple (2)
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Self-Paced Online, Classroom, Virtual Classroom
Medical Device Regulatory Requirements - (5 course bundle)
NSF International, Health Sciences
Bundle of 5 Courses - Medical Devices Regulatory Requirements. United States, Japan, Australia, Brazil, Canada A comprehensive overview of each...
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Professional Training
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10 hours
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From 1,400 USD
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Online
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Self-Paced Online
Medical Device Single Audit Programme (MDSAP)
International Professional & Industry Academy
The Medical Device Single Audit Program (MDSAP) was developed by the International Medical Device Regulators Forum (IMDRF) to conduct regulatory...
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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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Self-Paced Online
Medical Device Complaint Handling and Servicing
NSF International, Health Sciences
Maintaining proper Complaint files is an essential element of the medical device quality management system. This course will examine the...
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Professional Training
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1.5 hours
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From 300 USD
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Online
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Self-Paced Online
FDA Medical Device Reporting (MDR)
NSF International, Health Sciences
Medical Device Reporting is part of the Code of Federal Regulations - 21 CFR Part 803, mandated by Congress in...
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Professional Training
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1.5 hours
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From 299 USD
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Online
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Self-Paced Online
European Union Medical Device Regulation – EU MDR
5.0
(2)
NSF International, Health Sciences
In 2017, the Medical Device Regulation (EU MDR) 2017/745 was published, introducing major changes to the previous Medical Device Directive...
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Professional Training
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2 hours
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From 399 USD
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Online
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Self-Paced Online
ISO 13485:2016 – International Medical Device QMS Standard
NSF International, Health Sciences
This course provides in-depth instruction and expert clarification of ISO 13485:2016, the standard which serves as a basis for many...
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Professional Training
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2 hours
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From 400 USD
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Online
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Self-Paced Online
ISO 13485:2016 and the Medical Device Single Audit Programme
PTI
The publication of ISO 13485:2016 marked a turning point in Quality Management Systems for those involved in the life-cycles of...
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Professional Training
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5 weeks
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From 880 GBP
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Online
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Self-Paced Online
European Medical Device Regulation (EU MDR)- Understanding and Implementing the Requirements
NSF International, Health Sciences
This two-day course provides comprehensive instruction on the European Union Medical Device Regulation (EU MDR) 2017/745. The course walks students...
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Professional Training
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2 hours
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From 399 USD
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Online
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Self-Paced Online
MDSAP and Regulatory Transitions - The Basics Virtual Training
NSF International, Health Sciences
This course has been reviewed for technical accuracy as of March 2019. All contents are validated to current requirements as...
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Professional Training
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2 hours
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From 199 USD
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Online
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Self-Paced Online
Non-Conformance and Corrective Action for Medical Device Manufacturers
International Professional & Industry Academy
The identification of non-conformances and ensuring that they are dealt with in a timely and appropriate manner is a key...
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Professional Training
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From 299 GBP
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Online
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Self-Paced Online
European Union In-Vitro Diagnostic Device Regulation (IVDR)
NSF International, Health Sciences
In 2017, the In Vitro Diagnostic Device Regulation (EU IVDR) 2017/746 was published, introducing major changes to the previous In...
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Professional Training
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2 hours
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From 399 USD
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Online
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Self-Paced Online
Formulation and Processing Part 2 - QP Module
NSF International, Health Sciences
This intensive, interactive five-day pharmaceutical training course is designed to provide aspiring QPs and other pharmaceutical professionals with the knowledge...
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Professional Training
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5 days
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From 2,800 GBP
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Multiple (2)
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Self-Paced Online, Classroom, Virtual Classroom
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices
International Professional & Industry Academy
Sterile devices are free of viable microorganisms and the sterile barrier system is the key to maintaining this sterility until...
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Professional Training
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From 299 GBP
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Online
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Self-Paced Online
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