Healthcare and Medical Devices training

Training Courses for Healthcare and Medical Devices

Maximise your learning with TÜV SÜD experts

Maximise your learning with TÜV SÜD experts

Being up to date on the latest regulatory framework and requirements is vital for professionals in the healthcare and medical devices sector. 

With a global team of experienced healthcare and medical device experts, TÜV SÜD is well-positioned to equip you with the necessary knowledge and skills to navigate challenges faced by the sector that include technological advancements, increasing costs and changing regulations.

HOW WILL YOU BENEFIT FROM OUR healthcare & medical devices COURSES?
  • Build a solid foundation with an in-depth understanding of the subject through a curriculum curated by experts in the healthcare & medical devices sector
  • Reinforce your learning through case studies and interactive exercises
  • Clarify your doubts with our subject matter experts through live Q&A at our instructor-led training courses
  • Receive a globally recognised course completion certificate after successful completion of each course
  • Access to our community of experts for strategic guidance and continuous improvement
  • Know how to navigate the challenges in the healthcare & medical devices sector that include technological advancements, increasing costs and changing regulations

AVAILABLE healthcare & medical devices TRAINING COURSES

Awareness Program on Risk Management according to ISO 14971:2019 Standard

This 2-day training is to create awareness of the ISO 14971:2019 requirements and to have better understanding and implementation of risk management in the organisation.

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Awareness Program on Medical Device Regulation (EU) 2017/745

This 2-day training is to create awareness of MDR requirements and to have better understanding and implementation of MDR according to the EU’s initial framework in the 1990s.

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Process Validation & Software Validation for Medical Device

This 2-day training is to create awareness of the application of process validation within the medical device industry which is one of the key aspects to demonstrate compliance with both quality management systems for medical devices (EN) ISO 13485:2016 and intended statutory and regulatory requirements.

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Medical Device Single Audit Program (MDSAP)

This 2-day training is to help manufacturers acquire MDSAP audit program from registered body under MDSAP scheme to facilitate medical device registration and approval process by those destinated above regulatory countries.

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