Events and conferences

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: The TOPRA Symposium, held yearly since 2004, is the premier conference in Europe dedicated to healthcare regulatory affairs, with a programme encompassing the topics most relevant to those working in healthcare regulatory affairs, whether for human or veterinary medicines, medical devices or IVDs.

Speaker: Theresa Jeary

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: The TOPRA Symposium, held yearly since 2004, is the premier conference in Europe dedicated to healthcare regulatory affairs, with a programme encompassing the topics most relevant to those working in healthcare regulatory affairs, whether for human or veterinary medicines, medical devices or IVDs.

Speakers: Theresa Jeary

Speaking event: The conference will have representatives from domestic and foreign medical device regulatory agencies, medical device technology review agencies, international organizations that coordinate medical device regulations, and domestic and foreign standardization agencies.

Speaking event: The Xavier Health combination products community is led by top FDA officials and worldwide industry leaders who built the framework for the regulatory landscape of combination products.

Speaker: Theresa Jeary

Exhibition: world‑class plenary speakers, cross‑cutting educational programming, valuable networking and business development opportunities, The MedTech Conference is a must‑attend event for the industry’s prominent and most promising companies.

Exhibition: The annual symposium is Florida's premier event for medical device manufacturing firms, featuring nationally recognized speakers, expert panels on regulatory issues and industry trends, exhibiting companies, legislative updates and quality networking opportunities.

Webinar: 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. The primary requirements, which should be met, arise from the European Medical Device Regulation (MDR) itself and from the international standard IEC 62304 on software life cycle processes. In this event different views on (successful) agile medical software development will be provided.

Speaker: Bryan Pourciau

Speaking event: This 7th edition of MDG - MedGenerAction, explores the current regulatory landscape with representatives of a number of Notified Bodies, national experts and international representatives.

Speakers: Maddalena Pinsi

Speaking event: This is the fifth Regulatory Conference on the regulatory requirements for market authorisation of medical devices and in vitro diagnostics in Europe. Numerous internationally recognised experts from all thematically relevant fields will participate in the programme, including several Notified Bodies.

Speaker: Heike Möhlig-Zuttermeister

Speaking event: This conference will showcase how a risk-based approach can help guide an understanding of ways in which drug and device-led combination product categories may be similar and different, and how these attributes should inform product stewardship and regulation.

Speaker: Theresa Jeary

Speaking event: Complying with the new EU Requirements for IVD’s is expected to become very challenging for IVD manufacturers, some say even more than the MDR. The leaving point for many manufacturers is the IVD Directive that came into force in the year 2003. In the meantime, much has changed. This workshop will cover these big themes of the IVDR alongside with hands-on information on how to tackle the most important requirements.

Speakers: Erica Conway and Stefen Burde

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

Speaker: Jayanth Katta

Speaking event: The National Swiss MDR & IVDR conference are pleased to hold this year's national conference on the current topic of Switzerland as a Third Country. You can expect a varied programme with two plenary sessions, panel discussions, networking and six breakout sessions, each with a thematic focus.

Speaker: Heike Möhlig-Zuttermeister

Webinar: BSI hosts our tenth annual EU Medical Device Roadshow for the medical device manufacturer regulatory affairs, quality assurance and related consulting community. Join us for the virtual version of our Medical Device Roadshow exclusively focused on addressing European medical device regulatory and quality assurance requirements.

Exhibition: This is a must-attend event for the biopharma, medtech, diagnostic, and digital health industries wishing to do business in the region. This conference will feature the best companies from the southeast in the small company program and top-notch educational programming.

Exhibition: Medtech moves fast, especially in a healthcare hub like Minnesota. Keep the pace with the latest innovations and immerse yourself in a community of visionaries and industry leaders. It’s all waiting at the region’s most comprehensive medical design and manufacturing event — MD&M Minneapolis — part of Advanced Manufacturing Minneapolis.