Medqdoc
MedQdoc
Stay compliant and prepared for audits across ISO 13485, EU MDR, IVDR and FDA QSR. A validated, cloud-based eQMS that simplifies compliance and reduces time to market. ISO 13485:20
eqms software comparison: Stay compliant and prepared for audits across ISO 13485, EU MDR, IVDR and FDA QSR. A validated, cloud-based eQMS that simplifies compliance and reduces time to market. ISO 13485:2016 Certified
Stay compliant, in control and prepared for audits – across ISO 13485, EU MDR, IVDR and FDA QSR.
MedQdoc is a validated, cloud-based eQMS designed specifically for medical device and MedTech companies that need a structured, scalable quality management system – without unnecessary complexity or consultant dependency.
Buyer Snapshot
Best for
- Medical device companies seeking compliance with ISO 13485, EU MDR, IVDR, and FDA QSR.
- Organizations looking to streamline document control and improve audit readiness.
How engagement typically works
- Direct sales for demo requests and inquiries.
- Offers training programs for administrators and project teams.
Typical deliverables
- Validated, cloud-based eQMS software.
- Document Management module.
- Case Management module.
- Administrator and user training.
Good to know
- Best when integrated into existing quality and regulatory workflows for medical device compliance.
Pricing
Model:
Per user
HQ:
Grebbestad, Sweden
Languages:
English
Claim status:
Listed
Services & Capabilities
eQMS Software Comparison
Pricing model:
Per user
Deployment Model:
Cloud (SaaS)
Target Company Size:
Startup / Small team
Modules Included:
Document Control, Complaint Handling, Audit Management, CAPA, Change Control
Compliance Standards:
ISO 13485:2016, FDA QMSR (21 CFR Part 820), EU MDR/IVDR
Validation Pack Available:
Yes
Implementation Timeline:
Custom
Training Support:
Yes
Additional eqms_software_comparison Details
Deployment Model
Cloud (SaaS)
Target Company Size
Startup / SME / Mid-market
Modules Included
Document Management, Case Management
Compliance Standards
ISO 13485, EU MDR, IVDR, FDA QSR
Implementation Timeline
Custom
Pricing Model
Per user
