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Automated Regulatory Intelligence for MedTech and Life Sciences. It allows for continuous updates of regulatory...
Magazine
Discover the third edition of Ambit Iberia's Partner Insights Magazine with exclusive interviews, trend analysis,...
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QMSuite is a set of templates for a quality management system to help you manage...
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The Electronic Quality Management System (eQMS) becomes the natural evolution of the manual QMS. It's...
Magazine
An even deeper insight into the trends, innovations, and challenges that will shape the future...
Magazine
This magazine offers an in-depth look at innovation and the latest developments in the life...
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Service designed to automate calculations in chromatographic systems, optimizing the analysis process of compounds like...
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RaaSDesk is the new service from Ambit Iberia designed to provide the right support at...
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Our digital validation solution tackles challenges by fully digitizing validation processes. We offer an integrated...
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ManVa is a service dedicated to keeping the validation status of your cloud systems. At...
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Trust TraceDesk to keep your product traceability and optimize your supply chain efficiently and safely....
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Trust PRaaS to ensure the ongoing compliance of your IT systems and keep quality high...
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Animal Data Source is a fast, effective, and intuitive app that automates the process of...
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AReIA provides specialized support in controlled information searches related to technical standards, regulations, manufacturers, or...
Novedades sobre transformación digital de los sectores Farmacéutico, Biotecnológico y Dispositivos Médicos.
La revisión del MDR (Medical Device Regulation) reescribe la Regla 11 y el Reglamento Europeo de Inteligencia Artificial (AI Act) ya tiene calendario definitivo para la IA médica. Descubre en este artículo por qué la clase de tu software determina ...
Cuando un usuario abre un ticket porque una aplicación no responde, el problema puede haber comenzado mucho antes.
“La colaboración combina la experiencia de Ambit Iberia en consultoría especializada para Life Sciences con la capacidad técnica y regulatoria de Applus+ Laboratories para ofrecer un servicio integral a las compañías del sector Life Sciences.”
El entorno regulatorio de los dispositivos médicos está en constante evolución. Nuevas normativas, guías, estándares y actualizaciones de las autoridades competentes pueden afectar a los productos, procesos y documentación de las empresas.