Remediate. Medical Engineering. Radically.
Remedical is revolutionizing the MedTech industry with its innovative approach to medical equipment manufacturing. Focused on transforming operations for medical device manufacturers, Remedical offers CURA, an AI-powered SaaS platform that automates the entire lifecycle management process. This end-to-end solution integrates modules from design to post-market surveillance, significantly reducing manual effort and boosting productivity.
Located primarily in Zurich, CH, and with an additional presence at N Capital of Texas Hwy, Austin, Texas, US, Remedical is dedicated to providing solutions that are as precise and efficient as possible. By eliminating audit findings and driving operational excellence, Remedical is setting new standards in the MedTech sector. The company’s comprehensive platform ensures compliance and streamlines complex processes, enabling medical device companies to focus on innovation and growth.
Remedical is committed to taking MedTech operations to the next level through advanced technology and a customer-centric approach. With its focus on automation and efficiency, Remedical empowers medical device manufacturers to achieve unprecedented levels of productivity and quality. We invite the management team at Remedical to create a customized and exclusive company showcase and product listing on our platform to further enhance your market presence.
Compare Remedical with 3 companies in Medical-Equipment-Manufacturing
| Comparison Field |
RemedicalMain Company |
RYT Quality & Consul...View Profile |
Red MedtechView Profile |
IMed Consultancy LtdView Profile |
|---|---|---|---|---|
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Founded Year
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— | 0 | 2017 | 2012 |
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Company Size
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— | 2-10 | 2-10 | 11-50 |
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City
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Hadat, Beirut | Swansea, UK | Bloxham, England | |
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Country
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Lebanon | |||
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Skills & Keywords
Comparing with main company
|
29 Total Skills
Medical Equipment Manufacturing
MedTech
SaaS Platform
Lifecycle Management
Medical Devices
Regulatory Affairs
Automation
Complaint Handling
Risiko Management
Consulting
R&D
Development
Market Clearance
Design Control
ISO 9001
510k
ISO 14971
Post Market Surveillance
ISO 13485
Remediation
Risk Management
Medizintechnik
Compliance
Audit readiness
FDA
Project Management
Quality Assurance
Qualitätssicherung
SAAS
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19 Total
19 Unique
Unique Skills:
Adverse Events
Africa
Audit
CAPA
Central Asia
Complaints
+13
|
14 Total
14 Unique
Unique Skills:
CE mark projects
Consultancy
Design Assurance
Design History Files
Engineering
EU MDR
+8
|
16 Total
16 Unique
Unique Skills:
21 CFR Part 820
Auditing
CE Marking
Clinical Evaluations
Global Registrations
Health Canada
+10
|
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