Introduzione

The EU Medical Devices Regulation (MDR) 2017/745, together with evolving standards and guidance, introduces significant changes affecting the labelling of medical devices. These updates directly impact manufacturers’ regulatory strategies and product compliance activities.

This online training course provides participants with a clear overview of:

  • The regulatory requirements for medical device labelling under MDR.
  • The influence of guideline documents on labelling activities.
  • Practical preparation steps for achieving compliance from a regulatory labelling perspective.
  • Case study discussions to connect requirements with real-world applications.

By the end of the course, participants will gain a solid understanding of regulatory labelling requirements under MDR and learn how to implement hands-on strategies for compliance. The participants will be familiar with the new symbols of ISO 15223 and the latest version of ISO 20417, including their correlation with MDR and understand the latest developments in electronic Instructions for Use (e-IFU) regulations.

This training is designed to equip regulatory, quality, and labelling professionals with the knowledge and tools needed to ensure compliance and streamline labelling processes in today’s evolving MedTech landscape.

The training will be delivered in 2 parts, combining regulatory insights, practical guidance, and interactive discussion.

Part 1
Module 1: Overview of Labelling Requirements

  • MDD vs MDR – what has changed?
  • Labelling standards and guidelines
  • European and national laws
  • Latest developments in electronic Instructions for Use (eIFU)

Module 2: The MDR Requirements

  • MDR and the transition in a nutshell
  • What is new for labelling?
  • Risks of mislabelling
  • Notified Body expectations during audits

Part 2
Module 3: Preparing for MDR from a Labelling Perspective

  • General requirements (Annex I MDR)
  • Instructions for Use (IFU)
  • Label and sterile barrier considerations
  • UDI implementation & EUDAMED

Module 4: Symbols in Labelling

  • Benefits of using symbols
  • Symbols developed under MDR
  • National language requirements overview

Module 5: Case Study – System and Procedure Pack

  • Impact on UDI
  • Instructions for Use
  • Box information

Wrap-up

  • Summary and key recommendations
  • Knowledge check (quiz)
  • Interactive Q&A session
  • Regulatory Affairs
  • Labelling Department
  • Quality Assurance
  • Clinical Department
  • Marketing or Business Development responsible

Participant experience
Knowledge of the medical device directive MDD 93/42 is an advantage. Newcomers are welcome.

This training combines knowledge transfer with practical application to ensure participants gain both regulatory understanding and hands-on experience.

Docente/i
Arkan Zwick
Info

Arkan Zwick

Corporate Regulatory Affairs Director at CROMA Pharmaceutical, Austria

Mr. Arkan Zwick is Corporate Regulatory Affairs Director at a global pharmaceutical and surgical company active in ophthalmology, orthopedics, and aesthetic dermatology. With over 15 years of regulatory experience, he oversees EU compliance with notified bodies and manages global market authorizations across the Americas and Asia-Pacific. His expertise spans regulatory advocacy for drugs, medical devices, combination products, and cosmetics, as well as legal counsel on contracts, mergers & acquisitions, and intellectual property. Arkan holds a master’s degree in law and a PhD in European Law from the University of Vienna. He lectures in Vienna and speaks regularly at international conferences.

Online Training – 2 modules

MODULE 1 | 11 March 2026 from 2:30 to 5:30 pm CET
MODULE 2 | 12 March 2026 from 2:30 to 5:30 pm CET

After the registration, you will receive all details about the connection.

The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.

Early Bird: € 680,00* (until 18 February 2026)

Ordinary: € 875,00*

Freelance – Individual – Academy – Public Administration: € 495,00*

* for Italian companies: +22% VAT

The fee includes: tuitions, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.

Ilaria Butta
Ilaria Butta
Events & Training Manager
Versione Stampabile
Cosa saprai fare dopo il corso
Risultato atteso
Understand the content of the MDR 2017/745 and its specific impact on labelling requirements.
Risultato atteso
Achieve compliance with labelling obligations before the end of the transition period.
Risultato atteso
Apply practical insights and case study experience from industry practice.
Risultato atteso
Recognize Notified Body expectations during audits and technical dossier reviews.
Risultato atteso
Gain hands-on experience with high-risk devices and understand how to implement compliant labelling strategies in your company.
Risultato atteso
Stay up to date with the latest MDR developments and evolving requirements for electronic Instructions for Use (eIFU).
<p>Online interactive training on Zoom platform.</p> <p><em>LS Academy will provide the access link to the virtual platform a few days before the training.</em></p>

Online interactive training on Zoom platform.

LS Academy will provide the access link to the virtual platform a few days before the training.

<p>Online interactive training on Zoom platform.</p> <p><em>LS Academy will provide the access link to the virtual platform a few days before the training.</em></p>
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Labelling Requirements for Medical Devices