イベント・講演情報

Webinar: With the MDR and IVDR, European regulators need to ensure companies have a regulatory expert – a Person Responsible for Regulatory Compliance (PRRC) – at their disposal. This will ensure that the company is meeting certain specific EU requirements.

Exhibition: Digital Health will be the major driver of healthcare in the future – and this includes the medical technology industry. The event is designed to highlight and understand the key role of medical technology in the digitalisation of healthcare.

Speaking event: Join key stakeholders and decision makers across all intersections of the regulatory field for four powerful days of professional development, interactive discussions and relationship building.

Speaking event: National and international speakers will provide you with a detailed overview of the current legal framework in the European Economic Area. Learn how economic operators, Notified Bodies and authorities deal with the challenges of implementing the EU regulation.

Speakers: Heike Möhlig-Zuttermeister, Anna Mirabelli

Speaking event: Agile software development has become the state of the art in many companies. Due to the more flexible style of development, sometimes the question arises, if it is too flexible to meet strict regulatory requirements for medical devices.

Speaker: Bryan Pourciau

Speaking event: Connecting The MedTech Regulatory Community Through Expert Guidance, Interactive Discussions And Live Q&A. Benefit from Competent Authority, Notified Body and industry insights across 7 focused events: EU MDR. IVDR. EU Law. PMS. Clinical. Global Market Regulations. Biocompatibility.