Events Archive

If you are a Germany-based company with questions induced by the new MDR (classification, clinical testing & quality management of medical devices and in vitro diagnostics), this event is for you!

Together with our partners, we offer you an exclusive free check of your situation with regard to the new regulatory requirements.

During 1 hour, our Medidee experts will answer your questions and will guide you to the next steps!

Find out more and sign up for free: here

Hurry, slots go fast! First come, first served.

Medidee – Compliance with Relevance

If you are a Germany-based company with questions induced by the new MDR (classification, clinical testing & quality management of medical devices and in vitro diagnostics), this event is for you!

Together with our partners, we offer you an exclusive free check of your situation with regard to the new regulatory requirements.

During 1 hour, our Medidee experts will answer your questions and will guide you to the next steps!

Find out more and sign up for free: here

Hurry, slots go fast! First come, first served.

Medidee – Compliance with Relevance

Face the current Regulatory Framework with Confidence

Join our next seminar on November 11th, in Toledo, Spain, and get ready to face the current Regulatory Framework with confidence!

The Seminar „Basics of Regulatory Affairs in MedTech“ organized and led by Medidee’s expert consultants, aims to provide professionals in the field of Medical Devices with an introduction to the Regulations, Challenges and Good Practices that are necessary to comply with the current European Framework.

For who? Researchers and employees from start-ups, SMEs or any other company in the field of Medical Devices are welcome to join us at this event, conducted simultaneously in Spanish and English.

Entrance is free but places are limited, so make sure to register as soon as possible here.

If you are a Germany-based company with questions induced by the new MDR (classification, clinical testing & quality management of medical devices and in vitro diagnostics), this event is for you!

Together with our partners, we offer you an exclusive free check of your situation with regard to the new regulatory requirements.

During 1 hour, our Medidee experts will answer your questions and will guide you to the next steps!

Find out more and sign up for free: here

Hurry, slots go fast! First come, first served.

Medidee – Compliance with Relevance

The seminar „Medical Devices – Managing Current Regulatory Hurdles“ aims to provide MedTech industry professionals with exclusive insights into the European and Australian Medical Device and IVD Regulatory Environment.

With presentations from two leading global actors in the field, you will enjoy a rare opportunity to meet and hear from experts in the process of bringing a wide range of Medical Devices to market.

The event is followed by a networking session, where you will get the chance to interact closely with presenters and fellow industry professionals, further enriching your takeaways from this seminar.

More info about the program and registrations here.

Limited to 50 spots – Secure Yours Now!

We look forward to seeing you on March 9th in Sydney!

Êtes-vous une entreprise MedTech basée en France ? Avez-vous des questions à propos de la MDR, IVDR ou d’autres questions relatives au développement vos dispositifs médicaux ?

Profitez d’une heure gratuite de consultation avec nos experts ! Vous pourrez leur adresser toutes vos questions, concernant, par exemple, la classification de vos dispositifs, mais aussi les exigences d’évaluation clinique de dispositifs innovants, ou encore l’évaluation de votre positionnement réglementaire.

Nos experts seront à votre écoute !

Plus d’informations ici.

Réservez votre session gratuite sans attendre, seulement 8 créneaux sont prévus !

Medidee/Veranex will be part of the 6th Swiss Symposium in Point-of-Care Diagnostics, the successful event that brings medical, IVD industry, and research representatives together.

Our experts Dr Silvia Anghel, Dr Julianne Bobela, and Kim Rochat will be present among other speakers for a dedicated afternoon on Regulation and Investment related to Point of Care Diagnostics, on Wednesday, 25th of October 2023.

Get insights on the challenging aspects of regulations (In Vitro Diagnostic Regulation) and investment.

Learn more about the 1st Day program here

Book your ticket here

We look forward to meeting you there!