Autor
Daniel Tietjen

Dr. Daniel Tietjen

Partner

Read More
Autor
Daniel Tietjen

Dr. Daniel Tietjen

Partner

Read More

20. April 2021

Workshop: Medical Device Advertising – Compliance Aspects

  • Quick read
Medical device marketing would be wonderful if it weren’t for regulatory and compliance requirements to grind every claim beyond recognition. In addition, each EU country has slightly different marketing requirements for the Life Science industry, making it difficult to find one recipe for all. Moreover, a simple translation of your home market campaign will not do the job for markets abroad.

The law firm Taylor Wessing and Kalms Consulting have created an individual, half-day workshop for you to discuss your European marketing strategy from both compliance and strategy perspectives. We help you to identify the steps your marketing needs to be successful in Europe.

The workshop is designed as a half-day event and can be held as a regular face-to-face meeting or as an online event. It is dedicated to marketing, regulatory legal, compliance and management staff of healthcare companies who desire to enter the European market and who need an overview on relevant healthcare compliance topics.

To know more, download our PDF brochure here: Workshop: Medical Device Advertising – Compliance Aspects
Call To Action Arrow Image

Newsletter-Anmeldung

Wählen Sie aus unserem Angebot Ihre Interessen aus!

Jetzt abonnieren
Jetzt abonnieren

Related Insights

Coronavirus

COVID-19: Vertrieb von Schutzmasken – Ende der Sonderzulassungs-Praxis des BfArM

24. Juli 2020

von Dr. Daniel Tietjen

Klicken Sie hier für Details
Patents Technology & Life Sciences

Mögliche staatliche Zwangsmaßnahmen unter dem neuen IfSG und dem BayIfSG in Bezug auf medizinisches Material

15. April 2020

von Dr. Daniel Tietjen

Klicken Sie hier für Details
Patents Technology & Life Sciences

EU-Kommission empfiehlt Ausnahmen für Medizinprodukte und PSA zur COVID-19-Bekämpfung

23. März 2020

von Dr. Daniel Tietjen

Klicken Sie hier für Details