Cut Costs and Enhance Quality Processes With Dot Compliance - The Ready to Use, AI Powered eQMS. See Dot Compliance in action:https://lnkd.in/dUXHDe6c #eqms #qualitymanagement #qms #lifescience #qualitymanagementsystem
Dot Compliance
Software Development
Phoenix, Arizona 12,840 followers
Discover the Ready to Use, AI Powered QMS
About us
Dot Compliance is the first ready-to-use, AI-powered eQMS for Life Sciences. Packed with generative AI capabilities, Dot Compliance’s eQMS enables medical device manufacturers, biotechnology, and pharmaceutical companies to deliver to market faster and more cost-effectively.
- Website
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http://www.dotcompliance.com
External link for Dot Compliance
- Industry
- Software Development
- Company size
- 51-200 employees
- Headquarters
- Phoenix, Arizona
- Type
- Privately Held
- Founded
- 2016
- Specialties
- Compliance, 21 CFR Part 11, Quality Processes, SQM, Supplier Quality Management, Document Management, CAPA, Deviation, Adverse Event, Complaint, Regulatory Affairs and Registration, Training, Pharmaceutical, Medical Device, Cloud, Change Control, ECO, Validation, Quality Management, Quality Management System, Regulatory Compliance, Risk Management, FDA 510(k), Document Control, QMS software, ISO 13485, ISO 14971, FDA 21 CFR Part 820, FDA 21 CFR Part 11, and Quality System Regulations
Locations
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Primary
2375 E Camelback Rd
Suite 600
Phoenix, Arizona 85016, US
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2 Oppenheimer St
Rehovot, Israel 7670102, IL
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30 Old Bailey
London, England EC4M 7AU, GB
Employees at Dot Compliance
Updates
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Not sure how ISO 13485 and ISO 9001 differ? Our latest blog post explains what sets them apart and how each impacts your quality management approach. Learn the differences here: https://bit.ly/3zN0CEg #ISO13485 #ISO9001 #compliance #medicaldevices #qualitymanagement #eQMS
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Managing risks is key to ensuring product quality and compliance in the life sciences industry. In this blog post, we break down five essential steps for building a risk assessment framework that helps you identify, assess and, ultimately, manage top risks. Read the full blog post below 👇 https://bit.ly/4exoRoX #riskmanagement #riskassessment #qualitymanagement #lifesciences #eQMS
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💡 The September edition of our newsletter is out now! This month's newsletter is packed with practical insights on ISO 13485 compliance and quality management. From tips on preparing for your audit to improving medical device quality, we've got you covered. Plus, download our free ISO 13485 audit checklist to stay prepared. 📢 Don’t forget to stop by booth 15 at the American Medical Device Summit this week and join us on November 5th at Salesforce Tower London for a day of AI and compliance discussions. All the details inside ⤵
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The American Medical Device Summit is next week, and we can’t wait to connect with you! Don’t miss the chance to meet our team in booth 15 and discuss the impact of AI-powered quality and compliance on the medical device industry. Can't make it? Reach out for a demo and and see our solution in action. https://bit.ly/4ejFiVF #MedDeviceUS24 #GenerisAMD #DotCompliance #AI #Quality #MedicalDevice #RegulatoryCompliance
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📢 Mark your calendar for November 5th! Join us at the Dot Compliance Hub - London event at Salesforce Tower for a day of networking, exploring the latest in AI, and discussing best practices in compliance. Seats are limited, so don’t miss your chance to connect with industry experts and gain valuable insights. Secure your spot below! https://bit.ly/3zsM1xy #AI #Quality #Compliance #DotComplianceEvents
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Navigating the complexities of ISO 13485 can be a challenge, especially when preparing for an audit. Get deeper insights in our blog post, which breaks down the essential elements of ISO 13485 compliance. Whether you're new to the standard or looking to refine your quality management system, this guide has actionable insights to keep you on track. Check out the full post to ensure your organization is audit-ready! 👉 https://lnkd.in/eer_DZzq #ISO13485 #qualitymanagement #audit #compliance #medicaldevices #lifesciences
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We’re thrilled to be exhibiting at the American Medical Device Summit next month! Come meet our team of experts and let’s talk about the benefits of AI-powered quality and compliance. Can’t wait? Reach out today for a demo and get a sneak peek👇 https://bit.ly/4e8KonQ #MedDeviceUS24 #GenerisAMD #DotCompliance #AI #Quality #MedicalDevice #RegulatoryCompliance
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Dot Compliance reposted this
In the rapidly changing medical device industry, maintaining the highest quality standards is essential. Complaint management is crucial for identifying, addressing, and preventing issues related to product quality and patient safety. With advancing technology, the incorporation of artificial intelligence (AI) into quality management software solutions has become a game-changer. In Dot Compliance's recent blog, explore the benefits of using AI-integrated QMS for complaint management, and more. Read more: https://hubs.ly/Q02Q5MRm0 – #MedDeviceUS24 #GenerisAMD #DotCompliance #medicaldevice #AI #qualitymanagement
Revolutionizing Complaint Management in Medical Device with AI-Integrated Quality Management Software - Dot Compliance
https://www.dotcompliance.com
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💡 AI transforms pharmaceutical quality management by efficiently addressing challenges like regulatory compliance, supply chain disruptions, and complaint handling. Read our white paper to learn more about how pharmaceutical organizations can use AI to predict deviations, streamline complaint management, enhance supplier quality, and more. 👉 https://lnkd.in/e6qf2-xH #AI #Pharma #Quality #Compliance #eQMS