Request a Trial
Hoodin is specifically designed to perform monitoring for a life science product throughout their entire life cycle. With Hoodin, you have the flexibility to set up monitoring for a specific product (brand name) or a product type (such as a device, IVD product, or drug.) The trial project you will have access to will be customized to monitor the product or product type of your preference.
You will get access to a 14- day free trial of Hoodin
Request a Trial
Hoodin is specifically designed to perform monitoring for a life science product throughout their entire life cycle. With Hoodin, you have the flexibility to set up monitoring for a specific product (brand name) or a product type (such as a device, IVD product, or drug.) The trial project you will have access to will be customized to monitor the product or product type of your preference.
You will get access to a 14- day free trial of Hoodin
Request a Trial
Hoodin is specifically designed to perform monitoring for a life science product throughout their entire life cycle. With Hoodin, you have the flexibility to set up monitoring for a specific product (brand name) or a product type (such as a device, IVD product, or drug.) The trial project you will have access to will be customized to monitor the product or product type of your preference.
You will get access to a 14- day free trial of Hoodin
Webinar Gallery
AI Technology: For Regulatory Intelligence and Surveillance
Discover insights from our expert superpanel on AI's role in regulatory affairs. Gain knowledge on AI workflows, key concepts, policy implementation, and practical applications. Click here for all resources
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Join our RAQA Deep Dive session with Nicholas Wells to explore actionable insights and case studies on managing compliance challenges. Click here for all resources
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Empower yourself to transform adverse events into valuable lessons with our upcoming RAQA Deep Dives session led by expert Karolina Nożewska. Click here for all resources
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Dive into the critical role of biocompatibility in medical device safety with expert Marina Daineko as she unpacks essential strategies and insights in our latest deep dive session. Click here for all resources
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Discover the complexities of products classified as drugs in the US and devices in the EU with Veronika Valdova in this RAQA Deep Dives session. Click here for all resources
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Build a solid foundation in global regulatory landscapes and learn effective navigation strategies with Martin King in this RAQA Deep Dives session. Click here for all resources
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Get insights into regulatory obligations, risk management, and postmarket surveillance with our expert panelists on key topics for device companies in the EU and US. Click here for all resources