What can wedo for you?
We simplify access to regulated markets for health products for the well-being of patients.
MD101 collects and understands the needs of its customers to support them, pass on their know-how in order to bring them confidence and serenity in a market of increasing complexity.
MD101 promotes the membership of experts in a community that shares the same values, encourages the development and enhancement of their
skills and provide support in assignments and support to clients, in order to relieve them of administrative tasks, allow them to remain focused on their core business and promote their development in their self-employed status
This document presents the analysis of the regulatory strategy to be adopted for MultiDM, device intended for continuous monitoring of apnea at home
Renseignez votre e-mail pour recevoir le rapport completAll of our expertise
As a manufacturer of innovative medical technologies, you owe it to yourself to comply with applicable regulations. MD101 Consulting has a team of experts who will be able to guide you in the strategic choices and their implementation.
Our keyfigures
56
Formations au catalogue
21
Formateurs
93
Formations réalisées
704
Heures de formations réalisées
444
Participants aux formations
94%
De participants satisfaits
![Formation planifiée MD101 consulting : [21 et 22 mars 2023] : Appliquer les exigences de l’ISO 14971 dans le cadre du développement et de la mise sur le marché des Dispositifs Médicaux](https://www.md101consulting.com/wp-content/uploads/2022/06/Capture-decran-2022-10-11-a-10.24.47.png)
![Formation planifiée MD101 consulting : [3 et 4 avril 2023] : Pour lancer avec succès votre nouveau DM, préparez votre approche marketing en amont](https://www.md101consulting.com/wp-content/uploads/2022/10/strategie_legende.svg)
![Formation planifiée MD101 consulting : [12 et 13 avril 2023] : Appliquer les exigences de la norme IEC 62304 : 2006 + Amd1 au cycle de vie des logiciels](https://www.md101consulting.com/wp-content/uploads/2022/10/assurance_qualite_legende.svg)
![Formation planifiée MD101 consulting : [Analyse de risques] La place de l’analyse de risques dans le dossier technique (ISO 14971 et IEC 60601-1)](https://www.md101consulting.com/wp-content/uploads/2021/10/affaires-reglementaires-300x180.jpg)
![Formation planifiée MD101 consulting : [Affaires Cliniques] Règlement 2017/745/UE et ISO 14155 – la réglementation des investigations cliniques](https://www.md101consulting.com/wp-content/uploads/2022/06/Capture-decran-2022-10-11-a-10.24.00.png)
