Who is EUmediq?
EUmediq is Esra Gündağ's consultancy for medical device and drug-device regulation. It supports companies that manufacture medical devices in Türkiye and bring them to the European market, in areas such as MDR 2017/745 and CE marking, the ISO 13485 quality management system, clinical evaluation, risk management, validation and sterilization. The same expert runs each project from the first meeting to the close of the audit.
You can explore the site at eumediq.com.tr.
What's on the site?
- Home page: the main headline "Get your medical device ready for MDR and ISO 13485 audits," service summaries, an introduction to the expert and a three-step process (initial meeting, gap analysis, implementation and audit).
- Services: MDR and CE marking, ISO 13485, clinical evaluation (PMS, PMCF), vigilance, risk management (ISO 14971), validation and sterilization, biocompatibility (ISO 10993), marketing authorisation and GMP, supplier audits; each on its own page.
- About: areas of expertise, experience, who is supported and ways of working (project-based or ongoing consultancy).
- Contact: a form with a subject selector, phone and WhatsApp.
- English version: every page has its counterpart under
/en.
Highlights
Every service is a guide
The service pages don't stop at a short introduction. The MDR page explains, question by question and with an "On this page" table of contents, when the process is required, how classification is determined, which documents CE marking needs and how to move from MDD. Manufacturers can understand their own situation before talking to the consultant.
Contact that builds trust
The form ties each message to one of the nine services and asks up front for the details that make the first reply concrete. KVKK consent, an image verification code (with a question option for those who can't see it) and the option of an NDA before sharing documents are all stated clearly on the site. The cookie banner lets visitors continue with essential cookies only.
Analysis table
| Item | Status |
|---|---|
| Main heading (H1) | "Get your medical device ready for MDR and ISO 13485 audits" |
| Languages | 2 (TR, EN), linked with hreflang |
| Service pages | 9 per language |
| Sitemap | 28 URLs (September 2026) |
| Structured data | ProfessionalService, WebSite, Person, Service, BreadcrumbList |
| Lead capture | Form with subject selector + phone + WhatsApp |
| KVKK | Explicit consent, privacy notice, cookie preferences |
| Security | HTTPS + HSTS |
| Mobile | Responsive design |
For a similar project, see our corporate website, SEO and GEO and KVKK compliance services, and our healthcare and clinics and professional services pages for industry needs. From the same industry: GST Medikal and Disposet.
Which services does the EUmediq website cover?
MDR 2017/745 and CE marking, ISO 13485, clinical evaluation, vigilance, risk management, validation and sterilization, biocompatibility, marketing authorisation and GMP, and supplier audits, in Turkish and English.
Why do you explain services in so much detail on a consultancy website?
With technical subjects like regulation, clients look for information first. Detailed pages that answer their questions are found by search engines and AI tools, and they show expertise before the first meeting.