2026-03-22 2026-03-22 , online online, 225 € zzgl. MwSt. e-Learning: Medical Devices Basics - A Quick Introduction

Gain essential knowledge for your entry into the medical device industry in just 90 minutes! Understand regulations, market access, and vigilance with our compact e-learning.

Themen
  • European Medical Device Law and its Application in Germany
  • Definition of a medical device is and how it is brought to market
  • Vigilance / Market Observation (MD Monitoring and Reporting System)


Who should attend
  • Employees of medical device manufacturers and distributors with little or no experience in regulatory and quality affairs.
  • University graduates or young professionals with a medical or scientific background who want to prepare for a career in the regulatory and quality departments of medical device companies.
Ziel der Veranstaltung
Are you new to the MedTech industry or transitioning from another field?

Then our e-Learning is perfect for you! In three modules, you will learn the fundamentals of medical device regulations in EU and Germany, how medical devices enter the market, and how the reporting and monitoring system works.

Get a comprehensive overview in just 90 minutes!
Teilnehmerkreis

By the end of this e-learning, you will:

  • Understand the European medical device law and its application in Germany.
  • Be able to define what qualifies as a medical device and explain the process of bringing it to market.
  • Comprehend the vigilance system, including market observation, monitoring, and reporting requirements for medical devices.

26122541 e-learning: Medical Devices Basics: Medical Devices Basics - A Qu

Medical Devices Basics - A Quick Introduction

E-learning with 3 modules: Medical Device Law, Development and Conformity Assessment, Vigilance

Benefits
  • Up-to-date expert knowledge
  • Flexible learning at your own pace
  • Qualifying certificate
  • Practical examples and case studies
  • Official certification according to ISO 9001 and ISO 21001

Webcode 26122541

Jetzt buchen

JETZT Buchen

Alles auf einen Blick

Termin

anytime

anytime

Zeitraum

online

online
Veranstaltungsort

online

online

Downloads
PROSPEKT
PROSPEKT
Gebühr

Event - 225€ plus tax
Your personal single-user account is valid for 90 days from the date you receive your login details. During this period, you can revisit the modules as often as you like. Upon successful completion, you will receive a personalised, qualifying certificate. The participation fee includes all accompanying materials, further information, links, and templates. All materials are available for download.
Our General Terms and Conditions (as of 01.06.2024) apply, which we will send at any time upon request and which can be viewed on the Internet at https://www.forum-institut.com/cancellation-policy, as well as supplementary/different special conditions listed on each course website in individual cases.


Event - 225€ plus tax
Your personal single-user account is valid for 90 days from the date you receive your login details. During this period, you can revisit the modules as often as you like. Upon successful completion, you will receive a personalised, qualifying certificate. The participation fee includes all accompanying materials, further information, links, and templates. All materials are available for download.
Our General Terms and Conditions (as of 01.06.2024) apply, which we will send at any time upon request and which can be viewed on the Internet at https://www.forum-institut.com/cancellation-policy, as well as supplementary/different special conditions listed on each course website in individual cases.


Inhouse-Angebote
Inhouse-Angebot anfordern
Inhouse-Angebot anfordern

Jetzt buchen

Your contact

Verena Planitz
Conference Manager

+49 6221 500-655
v.planitz@forum-institut.de

Details

Gain essential knowledge for your entry into the medical device industry in just 90 minutes! Understand regulations, market access, and vigilance with our compact e-learning.

Themen

  • European Medical Device Law and its Application in Germany
  • Definition of a medical device is and how it is brought to market
  • Vigilance / Market Observation (MD Monitoring and Reporting System)


Who should attend
  • Employees of medical device manufacturers and distributors with little or no experience in regulatory and quality affairs.
  • University graduates or young professionals with a medical or scientific background who want to prepare for a career in the regulatory and quality departments of medical device companies.

Ziel der Veranstaltung

Are you new to the MedTech industry or transitioning from another field?

Then our e-Learning is perfect for you! In three modules, you will learn the fundamentals of medical device regulations in EU and Germany, how medical devices enter the market, and how the reporting and monitoring system works.

Get a comprehensive overview in just 90 minutes!

Teilnehmerkreis

By the end of this e-learning, you will:

  • Understand the European medical device law and its application in Germany.
  • Be able to define what qualifies as a medical device and explain the process of bringing it to market.
  • Comprehend the vigilance system, including market observation, monitoring, and reporting requirements for medical devices.