FAQ
Frequently Asked Questions
Practical answers to common questions about EU MDR 2017/745 compliance and the ReGentra platform.
Practical answers to common questions about EU MDR 2017/745 compliance and the ReGentra platform.
Last updated: May 2026
This notice explains how personal data is handled when you use the ReGentra website (regentramd.com) and submit information through the contact form. It is provided in line with the EU General Data Protection Regulation (GDPR) and the Turkish Personal Data Protection Law (KVKK).
Only the data you voluntarily provide through the contact form is collected: name, email address, and any optional information you choose to include (such as company, role, or a message). No cookies are used for tracking, and no third-party advertising or tracking pixels are present on this site.
The data is used solely to respond to your enquiry. It is not used for advertising or profiling, and it is not sold or shared with third parties for commercial purposes.
Form submissions are processed on ReGentra's own infrastructure, hosted within the European Union, and delivered to a ReGentra mailbox. Your data is not routed through third-party form-relay services, and it remains within EU infrastructure during normal operation.
Messages are retained only as long as needed to respond to and follow up on your enquiry. You may request deletion at any time.
Under GDPR and KVKK, you have the right to access, correct, delete, or restrict processing of your personal data, to object to processing, and to withdraw consent at any time. You also have the right to lodge a complaint with your local data protection supervisory authority. To exercise any of these rights, contact info@regentramd.com.
For any privacy-related questions or requests: info@regentramd.com
ReGentra is a regulatory technology system focused on the European medical device framework — specifically EU MDR 2017/745. It is currently available through a limited access program.
The content on this website is for informational purposes only and does not constitute regulatory, legal, or professional advice.
If you would like to learn more or request access, the contact form on the homepage is the appropriate way to get in touch.
All content on this site is provided for informational purposes only and does not constitute regulatory, legal, or professional advice. ReGentra makes no warranties regarding accuracy or suitability for any specific purpose; use of the information is at the user's own risk.
This site references publicly available regulatory frameworks and standards, including EU MDR 2017/745, MDCG guidance, and ISO/IEC standards. All such references remain the property of their respective publishers and rights holders. No content from copyrighted standards is reproduced verbatim on this site.
For any questions: info@regentramd.com