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# Zeliska

MedTech Consulting

## Sitemaps

- [XML Sitemap](https://zeliska.ch/sitemap.xml): Contains all public & indexable URLs for this website.

## Beiträge

- [Hello world!](https://zeliska.ch/hello-world/) - Welcome to WordPress. This is your first post. Edit or delete it, then start writing!

## Seiten

- [Home](https://zeliska.ch/) - ZELISKA. Services About Tools Micro-Consulting Swiss-Based MedTech Advisory Navigating MedTech Regulations Shouldn't Slow You Down. Expert, agile micro-consulting for ISO 13485, EU-MDR, and Medical Engineering. Get strategic, actionable compliance answers without the enterprise agency overhead. Solve a Bottleneck Now Explore Capabilities Framework_Scanner.sh System Ready // Select target framework & common obstacle: 1. Select Target Route
- [tools](https://zeliska.ch/tools/) - ZELISKA. Services About Tools Micro-Consulting GPMV Entscheidungshilfe Klassifizierung von Zwischenfällen Geltungsbereich Lädt... Ja Nein Reset Matrix ↺ MDR Risikoklassifizierung Klassifizierungsrechner (Annex VIII) Basis-Filter Lädt... Ja Nein Rechner zurücksetzen ↺ UDI-Anforderungs-Check Unique Device Identification (MDR/MepV) Basis-Filter Lädt... Ja Nein Check zurücksetzen ↺ © 2026 Zeliska. All rights reserved. Based in Switzerland.
- [About](https://zeliska.ch/about/) - ZELISKA. Services About Micro-Consulting Connect on LinkedIn System Audit Readiness Status: Secure Active: MAS Regulatory Affairs & Quality Management (Uni Bern) Infrastructure: FDA 510(k) Track Enabled "Engineering compliant pathways for complex medical devices." ISO 13485 // MDR // ISO 14971 Professional Experience & Education Ongoing MAS in Regulatory Affairs and Quality Management University of Bern
- [Glossary](https://zeliska.ch/glossary/) - [glossary]

## Kategorien

- [Uncategorized](https://zeliska.ch/category/uncategorized/)