About
MedQara, regulatory monitoring for medical devices
MedQara is an online (SaaS) platform for automated regulatory monitoring of medical devices and in vitro diagnostic devices. It picks up what authorities publish, summarises it, ranks it by criticality, filters it on each customer’s scope and keeps an exportable record for audits.
It is published by MedQara, a French sole proprietorship registered in the national business register (SIREN 108 783 465), based in Besançon. The platform has been in service since April 2026.
Key facts
- Category
- SaaS platform for automated regulatory monitoring, dedicated to medical devices (MDR, IVDR, FDA, ISO and IEC standards)
- Publisher
- MedQara, sole proprietorship, SIREN 108 783 465
- Head office
- 7 rue Pierre Laplace, 25000 Besançon, France
- In service since
- April 2026
- Sources
- 64 monitored sources, including 49 official authorities and institutions, covering 44 countries
- Frequency
- Collection every 6 hours
- Languages
- French and English
- Hosting
- European Union: database in Paris, application in Frankfurt
- Contact
- contact@veillemedqara.fr
How the monitoring is produced
Sources are official authorities and institutions (European Commission, MDCG, EUR-Lex, ANSM, HAS, Légifrance, FDA, MHRA, Swissmedic, ISO…) plus a few industry sources. Every alert links to the original text.
An AI model summarises each publication, ranks it (critical, moderate, info) and suggests the actions it calls for. The labels it assigns are checked against the source text before publication.
Each customer’s scope (device segments, standards, markets) filters the alerts and adjusts their criticality. Summaries help triage: they do not replace reading the official text.
Who it is for
- Medical device manufacturers and distributors: PRRCs, quality and regulatory affairs managers.
- QA/RA consultants and consulting firms, with one account that follows several clients.
- Hospital biomedical engineers, for materiovigilance and fleet follow-up.
What MedQara is not
- A consulting firm: MedQara does not write your files or represent you before authorities.
- A RIM platform: no submission management, country-by-country registrations or certificate management.
- A quality management system: MedQara feeds yours, it does not replace it.
Not to be confused with
MedQara (veillemedqara.fr) is independent of consulting firms with similar names, such as Med'In QARA, MIQARA Consulting or MEDQARA Consulting. It has no link with them.
Public pricing
Free account with no time limit, with a 48-hour delay. Independent €590 per year, Company €1,990 per year with unlimited users, Consultancy €3,900 per year for 10 clients, Group on quotation. 30-day trial.
See pricingFrequently asked questions
Who publishes MedQara?
MedQara, a French sole proprietorship registered in the national business register (SIREN 108 783 465), with its head office in Besançon. The legal notice gives the details.
Is MedQara a consulting firm?
No. It is online regulatory monitoring software. It has no link with consulting firms with similar names, such as Med'In QARA, MIQARA Consulting or MEDQARA Consulting.
Where does MedQara’s information come from?
From 64 sources, including 49 official authorities and institutions in 44 countries, collected every 6 hours. Every alert links to the original text.
How much does MedQara cost?
Free account with no time limit, with a 48-hour delay. Independent €590 per year, Company €1,990 per year with unlimited users, Consultancy €3,900 per year for 10 clients, Group on quotation. 30-day trial.