Your patient record is already your case report form.
- Dentists
- 11
- Cases enrolled
- 27
- Countries
- 9
- Average experience
- 25.2 years
Cases enrolled by country
Dentists by specialty
Years of experience
| Countries | Cases enrolled | Dentists |
|---|---|---|
| France | 8 | 2 |
| Turkey | 5 | 1 |
| Spain | 4 | 2 |
| Italy | 3 | 1 |
| Germany | 3 | 1 |
| Poland | 1 | 1 |
| Estonia | 1 | 1 |
| Croatia | 1 | 1 |
| Other | 1 | 1 |
An e-CRF built into the tool.
To collect clinical data, OralData offers several methods, including an e-CRF built into the software.
- For the dentist
- They fill in only one piece of software: the patient record is already the case report form.
- For industry
- Less monitoring and a much faster study, with a higher enrollment rate.
Data available in our database.
As of October 21, 2026
Real-world data, entered by dentists during care and structured in the patient record.
- patients
- 348,844
- procedures
- 544,566
- teeth
- 680,420
The database keeps growing: +2,174 patients and +3,409 procedures in one week.
For MDR and 510(k) submissions, clinical studies demonstrate the benefit-risk of medical devices.
Three documents to feed with clinical data
- CER
- Clinical Evaluation Report Ongoing clinical evaluation of the device.
- PMS
- Post-Market Surveillance Surveillance after the device is placed on the market.
- Clinical investigation
- Studies conducted to demonstrate performance and safety.
Frequently asked questions
All questions →What is an integrated e-CRF?
It is a clinical study's electronic case report form, built directly into the software: the patient record the dentist fills out is already the case report form.
What does the e-CRF change for the dentist?
They fill out a single piece of software, with no double data entry between their records and the study.
What does the e-CRF change for the company?
Less monitoring and a much faster study, with a higher inclusion rate.
Which regulatory documents is this data used for?
The clinical evaluation report (CER), post-market surveillance (PMS) and clinical investigations, for MDR as well as 510(k) submissions.
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