---
description: Detaillierte Informationen über Qualio zu Benutzerfreundlichkeit, Funktionen, Kosten, Vor- und Nachteilen aus verifizierten Nutzer-Erfahrungen. Lies Ratings & Bewertungen und entdecke ähnliche Tools.
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title: Qualio Erfahrungen, Vor- und Nachteile – Capterra Deutschland 2026
---

Breadcrumb: [Startseite](/) > [QM Software (Qualitätsmanagement)](/directory/30099/quality-management/software) > [Qualio](/software/134050/quality-management-software)

# Qualio

Canonical: https://www.capterra.com.de/software/134050/quality-management-software

Seite: 1 / 7\
Weiter: [Nächste Seite](https://www.capterra.com.de/software/134050/quality-management-software?page=2)

> QMS für medizinische Geräte, Pharma und Biotech. Vollständige FDA-/ISO-/GxP-Konformität. fünfmal schnellere Dokumentenkontrolle, Training, CAPA, NCRs, Audits und mehr.
> 
> Bewertung: **4.6/5** von 138 Nutzern. Top bewertet für **Weiterempfehlungsquote**.

-----

## Übersicht

### Wer verwendet Qualio?

Führende Mitarbeiter in Qualität \&amp; Compliance von Life Sciences Unternehmen (Biotechnologie, medizinische Geräte, Therapeutika, CxOs), die vor Compliance- und Regulierungs-Herausforderungen stehen (FDA, ISO, GxP) 

## Kurzstatistiken und Ratings

| Metrik | Bewertung | Detail |
| **Gesamt** | **4.6/5** | 138 Nutzerbewertungen |
| Bedienkomfort | 4.5/5 | Auf Basis der Gesamtbewertungen |
| Kundenbetreuung | 4.7/5 | Auf Basis der Gesamtbewertungen |
| Preis-Leistungs-Verhältnis | 4.4/5 | Auf Basis der Gesamtbewertungen |
| Funktionen | 4.3/5 | Auf Basis der Gesamtbewertungen |
| Empfehlungsprozentsatz | 80% | (8/10 Weiterempfehlungsquote) |

## Über den Anbieter

- **Unternehmen**: Qualio
- **Region**: San Francisco, USA
- **Gegründet**: 2010

## Gewerblicher Kontext

- **Zielgruppe**: 11–50, 51–200, 201–500, 501–1.000, 1.001–5.000, 5.001–10.000, 10.000+
- **Bereitstellungen und Plattformen**: Cloud, SaaS, webbasiert
- **Unterstützte Sprachen**: Deutsch, Englisch, Französisch, Italienisch, Spanisch
- **Verfügbare Länder**: Argentinien, Australien, Belgien, Brasilien, Chile, Deutschland, Dänemark, Ecuador, Finnland, Frankreich, Griechenland, Indien, Irland, Island, Italien, Japan, Kanada, Kolumbien, Luxemburg, Mexiko und 15 weitere

## Funktionen

- Alarmfunktion / Benachrichtigungen
- Alerts/Escalation
- Anpassbare Vorlagen
- Archivierung & Aufbewahrung
- Audit Trail
- Auditplanung
- Aufgabenmanagement
- Berichterstattung und Statistik
- Beschwerdemanagement
- Beurteilung-Management
- Compliance Management
- Compliance-Verfolgung
- Corrective and Preventive Action (CAPA)
- Dashboard
- Document Capture
- Dokumentenmanagement
- Dokumentenspeicher
- Dokumentkodierung & -kontrolle
- Elektronische Unterschrift
- Filesharing
- Formularverwaltung
- Genehmigungs-Workflow
- Geräte-Management
- Inspektions-Management
- Instandhaltungsmanagement
- Nachverfolgung von Nicht-Einhaltungen
- Planung ändern
- Qualitätskontrolle
- Richtlinien Managemen-
- Risikobewertung
- Risikomanagement
- Risk Analysis
- Störfallmanagement
- Suchen / filtern
- Third-Party Integrations
- Trainingsmanagement
- Ursachenanalyse
- Versionskontrolle
- Veränderungsmanagement
- Volltextsuche
- Werkzeuge zur Zusammenarbeit
- Wirtschaftsprüfung-Management
- Workflow-Management
- Zugriffskontrollen / Berechtigungen
- Überwachung

## Integrationen (27 insgesamt)

- Asana
- Azure DevOps
- Azure DevOps Labs
- Box
- ComplianceWire
- Confluence
- Elsevier Pure
- GitHub
- GitLab
- GitLab
- Google Workspace
- Google Workspace
- HubSpot CRM
- HubSpot Service Hub
- Jira

... und 12 weitere Integrationen

## Optionen für Kundensupport

- E-Mail/Helpdesk
- FAQ/Forum
- Wissensdatenbank
- Telefon-Support
- 24/7 Live-Support
- Chat

## Category

- [QM Software (Qualitätsmanagement)](https://www.capterra.com.de/directory/30099/quality-management/software)

## Ähnliche Kategorien

- [QM Software (Qualitätsmanagement)](https://www.capterra.com.de/directory/30099/quality-management/software)
- [Change-Management-Software](https://www.capterra.com.de/directory/30958/change-management/software)
- [Schulungsplattformen](https://www.capterra.com.de/directory/10008/training/software)
- [Compliance Software](https://www.capterra.com.de/directory/30110/compliance/software)
- [CAPA-Systeme (Corrective and Preventive Action)](https://www.capterra.com.de/directory/31343/corrective-and-preventive-action/software)

## Alternativen

1. [360Learning](https://www.capterra.com.de/software/211429/360learning) — 4.7/5 (515 reviews)
2. [Dot Compliance](https://www.capterra.com.de/software/192574/dot-compliance) — 4.4/5 (94 reviews)
3. [QT9 QMS](https://www.capterra.com.de/software/97557/qt9-quality-management) — 4.8/5 (125 reviews)
4. [Connecteam](https://www.capterra.com.de/software/153140/connecteam) — 4.6/5 (5317 reviews)
5. [Mitti (by SafetyCulture)](https://www.capterra.com.de/software/141080/iauditor) — 4.6/5 (355 reviews)

## Nutzerbewertungen

### "User friendly, sleek eQMS software" — 4.0/5

> **Dexter** | *3. August 2023* | Lebensmittelproduktion | Empfehlungsbewertung: 8.0/10
> 
> **Vorteile**: The software is very intuitive and easy to use.  We have little to no issues with implementation and understanding of how the system functions and documents/revisions move through the established workflows.  New employees and users are onboarded into the program with relative ease.
> 
> **Nachteile**: The pricing and user license tiers/packages could use a bit of rethinking.  It would be nice if Basic users (which are essentially read-only with access to Training and the Document Library only) did not take up a license from our annual subscription.Preferably, would like the user packages to be paid for only the Quality/Normal users that are actually creating and revising documents, or working on CAPAs, Nonconformances, Supplier Approval features, while Basic (read-only) users are able to login and view approved, effective documents for training purposes only without taking up a user license since they don't have access to the rest of the software's features.Other eQMS software and programs will have a separate training portal that can be accessed by any basic users without impacting the user licenses taken up.
> 
> The implementation and support team from Qualio are knowledgeable, courteous and extremely helpful with the onboarding and implementation process making for a very smooth transition.The support team is also very responsive and open to suggestions for changes to the software, and software versions are implemented quickly and efficiently to improve based on customer feedback and needs.

-----

### "A Great Quality Management System to get you started." — 5.0/5

> **Karl** | *15. August 2023* | Pharmazeutika | Empfehlungsbewertung: 7.0/10
> 
> **Vorteile**: Qualio has a great user interface for anyone needing to create, edit, review, find and extract documents from a reliable document control system.  This experience also spills over to their events module allowing me to personalise an audit and risk functionality that fit the mould of my companies quality journey.  The Customer Service both supporting the induction of the platform and the every day query customer service is outstanding and could not compliment them more.  The Help features of the platform make it easy for me to find quick assistance on what I need to do and the regular webinars are a blessing for me to understand what is in production to improve my experience with Qualio.  Sandbox environment is great and much welcomes to play around before doing something you will regret in the live environment.
> 
> **Nachteile**: Qualio still have some sticking points with the document creation journey and while they are improving every day, they are still sorely lacking ease with the creation, reviewer and approval experience.  Supplier event is also brand new and not quite the finished product yet.  But its heading in the right direction.
> 
> I have been with Qualio for more than a year now and my company have bought into their first Quality Management System for the first time thanks to Qualios fantastic interface and ease of use.  That is the priority for any QMS.

-----

### "Perhaps fine for some industries" — 2.0/5

> **Christina** | *3. Mai 2026* | Medizinische GerÃ¤te | Empfehlungsbewertung: 1.0/10
> 
> **Vorteile**: It seemed easy to implement. I also liked the feature where all words can be searched in controlled documents.
> 
> **Nachteile**: It wasn’t compliant enough for pharma/med device. I began validating the system and found that controls weren’t in place.
> 
> It was not my favorite. When I identified issues, the customer care team stopped responding. I think they have a good start to a platform; but they need to work on compliance and customer care.

-----

### "Customer Questionnaire" — 5.0/5

> **Lowell** | *8. August 2023* | Medizinische GerÃ¤te | Empfehlungsbewertung: 10.0/10
> 
> **Vorteile**: Aesthetically pleasing, Ease of use, ease of support, at a competitive cost. Qualio meets all expectations. Qualio gives us the ability to work remotely. This seems like the norm since Covid but the last few years cannot erase generations of employees being required to be in a brick in mortar location to work. Having our products available throughout the world keeps a little stability during a US economic downturn.
> 
> **Nachteile**: There is not a well defined way to get feedback to the Qualio team for improvement suggestions. The Qualio has addressed my ideas but there needs to be a ticket system with feedback from the suggestion. This just needs to be addressed as a system. A ticker could be made in Qualio and assigned to the IT department. The idea can be approved or denied. The ticket can be closed. Super simple.
> 
> 100% document implementation into Qualio. Internal and third party audits directly from Qualio. Complete integration into Qualio for SD team and the sales and marketing team.

-----

### "Qualio as a Quality Management Software" — 5.0/5

> **David** | *3. August 2023* | Medizinische GerÃ¤te | Empfehlungsbewertung: 8.0/10
> 
> **Vorteile**: User interface and scalability/adaptability to business needs
> 
> **Nachteile**: Inability to lock values and text fields in Events and documents.  Inability to run reports, or export data for tracking/reporting outside of Qualio.  Interface with other data sets.

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Seite: 1 / 7\
Weiter: [Nächste Seite](https://www.capterra.com.de/software/134050/quality-management-software?page=2)

## Links

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