Healthcare & Medical Devices


NAVIGATING THE HEALTHCARE & MEDICAL DEVICES INDUSTRY: ENHANCE YOUR SKILLS WITH TÜV SÜD'S TRAINING COURSES

Discover more about our Healthcare & Medical Devices training courses, where we focus on the importance of staying up to date on the latest regulatory framework and requirements for professionals in the healthcare and medical devices sector. With a global team of experienced healthcare and medical device experts, TÜV SÜD is well-equipped to provide you with the necessary knowledge and skills to navigate the challenges faced by the sector, including technological advancements, increasing costs, and changing regulations. Join us and take your career in the medical devices industry to the next level.

1 - 12 of 20 Results
Healthcare & Medical Devices
Internal Auditor Training Program on Primary Packaging Materials for Medicinal Products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) based on ISO 15378:2017

Face-to-face Training02 DaysIntermediate
Healthcare & Medical Devices
Internal Auditor Training Program on Medical Devices - Quality Management System based on ISO 13485:2016 integrated with EU MDR requirements.

Face-to-face Training3 DaysIntermediate
Healthcare & Medical Devices
Training Program on Safety & EMC Requirements of Medical Devices based on IEC 60601-1-1, IEC 60601-1-2

Face-to-face Training2 DaysIntermediate
Healthcare & Medical Devices
Implementation Training Program on Medical Devices - Quality Management System based on ISO 13485:2016

Face-to-face Training2 DaysIntermediate
Healthcare & Medical Devices
Training Program on ASEAN Product Registration and Regulatory Bodies in the Region - Medical Devices

Face-to-face Training1 DayIntermediate
Healthcare & Medical Devices
In Vitro Diagonistic Medical Devices Regulation (IVDR)

Self-paced Learning105 minsBeginnerE-learning
Healthcare & Medical Devices
Awareness Training Program on Primary Packaging Materials for Medicinal Products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) based on ISO 15378:2017

Face-to-face Training01 DayBeginner
Healthcare & Medical Devices
Post Market Surveillance under IVDR (2017/746)

Face-to-face Training1 DayIntermediate
Healthcare & Medical Devices
Training Program on Medical Device Software Compliance Requirements

Face-to-face Training1 DayIntermediate
Healthcare & Medical Devices
Awareness Training Program on IVD Regulation – (EU) 2017/746 for In Vitro Diagnostic Medical Devices

Face-to-face Training2 DaysBeginner
Healthcare & Medical Devices
Training Program on Application of Usability Engineering to Medical Devices based on IEC 62366-1:2015

Face-to-face Training2 DaysBeginner
Healthcare & Medical Devices
Fundamentals of Medical Device Single Audit Programme (MDSAP)

Self-paced Learning105 minsBeginnerE-learning

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