Compliance made available for Pre-Market Companies
Simplify, digitalize, and accelerate your regulatory processes:
Gain faster and more cost-efficient introduction of innovative products to the market.
The platform is built to meet the needs of both bigger and smaller companies because they must fulfill the same MDR, GDPR, FDA and ISO requirements.
– Kenn Milton, Founder & CEO at MyBlueLabel
100% faster implementation
Use 75% less time and money becoming compliant
All modules are available from day 1
Use prewritten templates to comply with ISO standards
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MyBlueLabel’s platform is based only on internationally recognized Quality Management standards. Combined with industry expertise in Life Science, Software Validation and Risk Management means that with MyBlueLabel’s QMS you can manage regulatory requirements from launching a new product and even managing post-market activities. All in the same platform.
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MyBlueLabel dashboards are used for visual display of the project portfolio activities. From the dashboard you have the possibility to see which projects are on track, needs attention or are off track. By selection it is feasible to get the project status of the entire company or per organizations in one view.
The Dashboards are all clickable which enables you to filter and find information with the click of a buttom.
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Integrate with your existing systems to ensure a seamless transition. We provide a tailored platform with real-time metrics and user-friendly navigation.
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MyBlueLabel has a suite of modules to support the full ecosystem of processes to comply with regulations and international standards. The modules are integrated or can work as standalone modules.