Date
Post Date
july 2022
![Regulatory Check Up - Germany](https://medidee.com/wp-content/uploads/2022/01/16.png)
Event Details
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
Event Details
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
Time
(Tuesday) 9:00 am - 4:00 pm CEST
Location
Online Event
august 2022
![Regulatory Check Up - Germany](https://medidee.com/wp-content/uploads/2022/01/17.png)
Event Details
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
Event Details
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
Time
(Tuesday) 9:00 am - 4:00 pm CEST
Location
Online Event
![CARAQA program at HEIG-VD, Switzerland - online info session on Aug. 22th 2022](https://medidee.com/wp-content/uploads/2022/08/CARAQA-posts-1.png)
Event Details
Your last chance to ask all your questions! Free online info session to discover CARAQA program in Yverdon-les-Bain, on August 22th Evolve towards your company’s decision-making centers and play a
Event Details
Your last chance to ask all your questions! Free online info session to discover CARAQA program in Yverdon-les-Bain, on August 22th
Evolve towards your company’s decision-making centers and play a key role in maintaining your company’s competitiveness and sustainability, faced with regulatory challenges.
Join this 6 months program to become a Clinical Affairs, Regulatory Affairs & Quality Assurance specialist for Medical Devices and IVDs.
During 1 hour, Didier Maillefer from HEIG-VD and Elena Lucano from Medidee will tell you more about this CARAQA program in Yverdon-les-Bains, Switzerland, offered in partnership with HEIG-vd, Haute Ecole d’ingénierie et de gestion, from the canton of Vaud.
Next starting date is in September 2022, want to know more?
Join us on August 22th at 5:30 PM CEST. Teams link is coming soon!
Time
(Monday) 5:30 pm CEST
Location
Online Event
Organizer
HEIG-VD
september 2022
05sep4:00 pm[WEBINAR] Build compliant Technical Documentation (TD) under MDR4:00 pm CEST
![Technical Documentation Webinar - September 5th - Medidee Services](https://medidee.com/wp-content/uploads/2022/08/Mdd-Webinars.jpg)
Event Details
[WEBINAR] Build compliant Technical Documentation (TD) under MDR Did you know it takes between 6 and 18 months from application to issuance of the MDR certificate for 80% of the companies? Did
Event Details
[WEBINAR] Build compliant Technical Documentation (TD) under MDR
Did you know it takes between 6 and 18 months from application to issuance of the MDR certificate for 80% of the companies?
Did you know 50% of the submitted TD are incomplete at first?
To expedite the Technical Documentation review process by the Notified Body and avoid extra costs and delays (which potentially could make your company miss the May 2024 deadline), your technical documentation submission needs to be right the first time!
Medidee supports your MDR transition process. During this webinar, our experts Lydie Moreau and Philippe Etter will tell you all about:
– What are the additional requirements of MDR compared to previous directives
– What is the structure your TD should comply to
– How to make sure you have a clear traceability thread within your TD to demonstrate compliance to all GSPRs
Interested in joining us? Register here!
Time
(Monday) 4:00 pm CEST
Location
Online Event
![CARAQA Muttenz - Info Session on Sept. 6th](https://medidee.com/wp-content/uploads/2022/08/CARAQA-posts-1-1.png)
Event Details
Free info session to discover CARAQA program in Muttenz on September 6th Progress towards your company’s decision-making centers and play a key role in maintaining your company’s competitiveness and
Event Details
Free info session to discover CARAQA program in Muttenz on September 6th
Progress towards your company’s decision-making centers and play a key role in maintaining your company’s competitiveness and sustainability while successfully navigating all the regulatory challenges.
Join this 6 months program to become a Clinical Affairs, Regulatory Affairs & Quality Assurance specialist for Medical Devices and IVDs.
During 1:30, David Hradetzky from FHNW and Philippe Etter from Medidee will tell you more about this CARAQA program in Muttenz, Switzerland, offered in partnership with FHNW, The University of Applied Sciences and Arts from the Northwestern Switzerland.
Next starting date is in January 2023, want to know more?
Reserve your seat now and join us on FHNW Campus on September 6th from 6 to 7:30PM CEST.
Book your seat here.
Time
(Tuesday) 6:00 pm - 7:30 am CEST
Location
Campus Northwestern Switzerland University of Applied Sciences (FHNW)
![CARA Muttenz - Info Session - 2022.09.06](https://medidee.com/wp-content/uploads/2022/05/CARAQA-posts-4.png)
Event Details
Join us live on FHNW Muttenz Campus for the next CARAQA FHNW Info session on September 6th! Prepare yourself for the next CARAQA program which will start in January 2023! Philippe
Event Details
Join us live on FHNW Muttenz Campus for the next CARAQA FHNW Info session on September 6th!
Prepare yourself for the next CARAQA program which will start in January 2023!
Philippe Etter and David Hradetzky will present you the program and answer all your questions.
Be part of the next CARAQA Muttenz class and become a Clinical Affairs, Regulatory Affairs, and Quality Assurance specialist with this recognized training!
Our Certificates of Advanced Studies is sponsored by Swiss Medtech and Medidee.
Click here to book your seat for the Info session
For additional info on all our programs, visit Caraqa’s website
Contact us for any request at training@medidee.com
Time
(Tuesday) 6:00 pm - 7:30 pm CEST
Location
Campus Northwestern Switzerland University of Applied Sciences (FHNW)
![Regulatory Check Up - Germany](https://medidee.com/wp-content/uploads/2022/01/18.png)
Event Details
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
Event Details
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
Time
(Tuesday) 9:00 am - 4:00 pm CEST
Location
Online Event
![CARAQA program UCLouvain - Info Session, Sept. 29th](https://medidee.com/wp-content/uploads/2022/09/CARAQA-posts.png)
Event Details
CARAQA UCLouvain online info event Join us on September 29th at 5:00 PM to learn more about the CARAQA program in Belgium! Progress towards your company’s decision-making centres and play a key
Event Details
CARAQA UCLouvain online info event
Join us on September 29th at 5:00 PM to learn more about the CARAQA program in Belgium!
Progress towards your company’s decision-making centres and play a key role in maintaining your company’s competitiveness and sustainability while successfully navigating all the regulatory challenges.
Be part of the 4th edition CARAQA UCLouvain in Belgium, and become a Clinical Affairs, Regulatory Affairs, and Quality Assurance specialist with this recognised training.
Next starting date is 13th January 2023, want to know more? Elena Lucano, Pierre Geens and Renaud Ronsse will answer all your questions about the program.
Click here to access to event page, and confirm your attendance.
Contact us for any request at hello@caraqa.com
Time
(Thursday) 5:00 pm - 6:00 pm CEST
Location
Online Event
october 2022
![Regulatory Check Up - Germany](https://medidee.com/wp-content/uploads/2022/01/19.png)
Event Details
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
Event Details
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
Time
(Tuesday) 9:00 am - 4:00 pm CEST
Location
Online Event
november 2022
![Regulatory Check Up - Germany](https://medidee.com/wp-content/uploads/2022/01/20.png)
Event Details
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
Event Details
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
Time
(Tuesday) 9:00 am - 4:00 pm CET
Location
Online Event
11novAll Day[SEMINAR] "Basics of Regulatory Affairs in MedTech"(All Day: friday) CET Région:Spain
![Seminar](https://medidee.com/wp-content/uploads/2022/10/Mdd-Webinars-1.png)
Event Details
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
Event Details
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.
Time
All Day (Friday) CET
Location
Hospital Nacional de Parapléjicos - Toledo, Spain
december 2022
![Regulatory Check Up - Germany](https://medidee.com/wp-content/uploads/2022/01/21.png)
Event Details
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
Event Details
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
Time
(Tuesday) 9:00 am - 4:00 pm CET
Location
Online Event
january 2023
No Events
february 2023
No Events
march 2023
![](https://medidee.com/wp-content/uploads/2023/02/Sydney-regulatory-seminar-1-1.png)
Event Details
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
Event Details
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!
Time
(Thursday) 4:00 pm - 8:00 pm Sydney Time
Location
Rydges World Square Sydney 389 Pitt Street Sydney NSW 2000
april 2023
No Events
may 2023
No Events
june 2023
No Events
july 2023
No Events
august 2023
No Events
september 2023
![](https://medidee.com/wp-content/uploads/2023/08/RCU-France-2.png)
Event Details
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
Event Details
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 !
Time
(Thursday) 9:00 am - 4:30 pm CEST
Location
Online Event
october 2023
![](https://medidee.com/wp-content/uploads/2023/08/swiss-symposium-poc-diagnostics.png)
Event Details
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
Event Details
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!
Time
(Wednesday) 2:00 pm - 6:00 pm CEST
november 2023
No Events
december 2023
No Events
january 2024
No Events
february 2024
No Events
march 2024
No Events
april 2024
No Events
may 2024
No Events
june 2024
No Events