Discover the Ready to Use, AI Powered QMS
Dot Compliance is a leading software development company revolutionizing the Life Sciences industry with its ready-to-use, AI-powered eQMS (Electronic Quality Management System). Designed to accelerate time-to-market and reduce costs, Dot Compliance empowers medical device manufacturers, biotechnology firms, and pharmaceutical companies with cutting-edge generative AI capabilities.
Located at Primary: 2375 E Camelback Rd Suite 600 Phoenix, Arizona 85016, US, and with additional offices at 2 Oppenheimer St Rehovot, Israel 7670102, IL and 30 Old Bailey London, England EC4M 7AU, GB, Dot Compliance specializes in providing solutions for FDA 21 CFR Part 11, Change Control, Deviation, Adverse Event, and comprehensive Quality Management. The company's expertise extends to ECO, Document Management, Training, and Supplier Quality Management, ensuring seamless regulatory compliance and optimized quality processes. Dot Compliance delivers unparalleled value and innovation to its clients.
By focusing on cloud-based solutions and integrating the latest advancements in AI, Dot Compliance continues to set new standards in quality management systems. Discover how Dot Compliance can transform your quality processes and drive unprecedented efficiency. We invite the management team of Dot Compliance to create a customized and exclusive company showcase and product listing on our platform to further amplify their reach and impact.
Compare Dot Compliance with 3 companies in Software-Development
| Comparison Field |
Dot ComplianceMain Company |
Greenlight GuruView Profile |
UnifizeView Profile |
QualioView Profile |
|---|---|---|---|---|
|
Founded Year
|
— | 2013 | 2019 | 2012 |
|
Company Size
|
— | 201-500 | 11-50 | 51-200 |
|
City
|
Phoenix, Arizona | Indianapolis, Indiana | Palo Alto, California | San Francisco, California |
|
Country
|
United States | United States | United States | United States |
|
Skills & Keywords
Comparing with main company
|
33 Total Skills
eQMS
AI Powered QMS
Life Sciences
Regulatory Compliance
Quality Management System
Medical Device
Pharmaceutical
FDA 21 CFR Part 11
Change Control
Deviation
Adverse Event
Quality Management
ECO
Document Management
Training
Supplier Quality Management
Validation
FDA 21 CFR Part 820
ISO 14971
FDA 510(k)
ISO 13485
Compliance
21 CFR Part 11
Quality Processes
SQM
CAPA
Complaint
Regulatory Affairs & Registration
Cloud
Risk Management
Document Control
QMS software
Quality System Regulations
|
9 Total
9 Unique
Unique Skills:
Clinical Data
Clinical Data Capture Software
Clinical Investigations
Design Control
EDC System
Electronic Data Capture (EDC)
+3
|
25 Total
2 Common
23 Unique
Match
6%
Common Skills:
eQMS
Life Sciences
Unique Skills:
Aerospace & Defense
AS9100
Automotive
Biotechnology
Cosmetics
Design Control
+17
|
23 Total
1 Common
22 Unique
Match
3%
Common Skills:
eQMS
Unique Skills:
BioTechnology
Cannabis
Contract Research Organizations
CRO
Design Control
Document Control Software
+16
|
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