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Description
Ensuring that business processes are free of defects results in the creation of products without flaws. This is precisely why CASQ-it has been developed to cover every phase of your quality assurance and management procedures, beginning with the development stage and extending through material handling, all the way to support processes. The strength of CASQ-it is found in its process-oriented approach, offering a feature that allows your CAQ system to adjust seamlessly to your specific workflows rather than forcing your operations to conform to it. CASQ-it paves the way for your quality assurance efforts to advance into the future, enhancing quality and reliability, which in turn boosts customer satisfaction and lowers quality-related costs. Each CASQ-it module operates independently, allowing for the immediate optimization of distinct processes and workflows within your organization. Moreover, these modules can be combined in various ways, or utilized to form a holistic quality assurance framework tailored to your needs. Embracing this flexibility facilitates continuous improvement and fosters innovation within your quality management practices.
Description
RQM+ stands as a prominent global provider of medical technology services, dedicated to accelerating compliance and ensuring market success for its clients. With a wealth of expertise and deep industry insight, we offer tailored solutions that streamline the entire product lifecycle for medical technology firms, guiding them from initial concept through to commercialization and beyond. Our comprehensive suite of services facilitates seamless end-to-end solutions that encompass every stage of the medical device development process. The quality assurance engineers at RQM+ meticulously evaluate material lists, establish supplier networks, and assist in navigating the design change process. Likewise, our design quality engineers are instrumental in overseeing crucial aspects such as packaging, sterility, biocompatibility, and required device testing. Our regulatory affairs consultants play a vital role by providing expert guidance and assistance with submissions to the FDA, notified bodies, and other regulatory agencies. Additionally, we leverage our significant experience with current reimbursement requirements and value-based compensation frameworks to enhance our clients' market positioning. Ultimately, RQM+ is committed to empowering medical technology companies to achieve their goals efficiently and effectively.
API Access
Has API
API Access
Has API
Integrations
No details available.
Integrations
No details available.
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
BÖHME & WEIHS
Founded
1985
Country
Germany
Website
www.boehme-weihs.de/en/
Vendor Details
Company Name
RQM+
Country
United States
Website
www.rqmplus.com
Product Features
Audit
Alerts / Notifications
Audit Planning
Compliance Management
Dashboard
Exceptions Management
Forms Management
Issue Management
Mobile Access
Multi-Year Planning
Risk Assessment
Workflow Management
Quality Management
Audit Management
Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Defect Tracking
Document Control
Equipment Management
ISO Standards Management
Maintenance Management
Risk Management
Supplier Quality Control
Training Management
SPC
Corrective Actions (CAPA)
Data Entry
Data Linking
Data Management
Excel Loader
Job Management
OPC Data Collection
Performance Metrics
Point-of-Production Analysis
Real Time Data Collection
Regulatory Compliance