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Medical devices need proper storage to stay safe and effective. For business to understand what storage requirements their products need, it's important to understand what FDA class your device falls under. Learn more about medical devices and what to look for in a storage partner on our blog here:?https://lnkd.in/gV7ffWsT To learn more about medical device classes, check out the FDA's product classification database: https://lnkd.in/e4junhtS #3PL #MedicalDevices #Healthcare

Curious about PFAS and medical devices? If you're headed to Chicago for the American Medical Device Summit, be sure to stop by booth 54 to chat with Shalene Thomas about how #PFAS regulations are impacting the #medicaldevice industry and what you need to know. Not able to attend? Register for our upcoming webinar "PFAS in Medical Devices: Ask An Expert". https://okt.to/dYObuX #MedDeviceUS24 #GenerisAMD #MedicalDevices #MedicalDeviceSolutions

Watched by the top medical device manufacturers in 2024—and here’s why! Reprocessing validations are essential to ensure that medical devices are safe for the intended use and reuse. In this on-demand webinar, Christine Laube, Technical Advisor at TüV SüD, breaks down what you need to know: * Understanding ST98 * How the latest standards impact manufacturers * Best practices that can be implemented in your operations ?? Watch the webinar now: https://spkl.io/6049fbtNl #MicrobiologyTesting #MedicalDevices #Reprocessing

We hear you… certain activities required by the FDA may feel like a waste of time ??, leading to frustration. However, it’s important to consider the "why" behind these, especially in the context of medical device development. We want to help you navigate and streamline these activities—check out our article “Why Are You Wasting Time Building Your Medical Device?” to learn more: ?? https://hubs.li/Q02NgGH10 Heading to RAPS Convergence 2024? We'd love to connect! ?? Stop by Booth #825 and let's discuss how we can help. See you there! ?? #MedicalDevices #HealthTech #MedicalSoftware #FDA #SaMD #SoftwareDevelopment #RAPSConvergence #RegulatoryCompliance

We hear you… certain activities required by the FDA may feel like a waste of time ??, leading to frustration. However, it’s important to consider the "why" behind these, especially in the context of medical device development. We want to help you navigate and streamline these activities—check out our article “Why Are You Wasting Time Building Your Medical Device?” to learn more: ?? https://hubs.li/Q02PMBDH0 Heading to RAPS Convergence 2024? We'd love to connect! ?? Stop by Booth #825 and let's discuss how we can help. See you there! ?? #MedicalDevices #HealthTech #MedicalSoftware #FDA #SaMD #SoftwareDevelopment #RAPSConvergence #RegulatoryCompliance

Staying up to date with regulations and also understanding their impacts is one of the bigger challenges in the medical device industry. ?? But what if you had a way to not only stay up-to-date but also understand complex regulations with ease? That’s where Elly’s News Feature steps in! ?? ?? Curious to see how it works? ?? Watch the video below to learn more! www.regulationagent.com #regulatoryglobe #mdr #medizinprodukte

We hear you… certain activities required by the FDA may feel like a waste of time ??, leading to frustration. However, it’s important to consider the "why" behind these, especially in the context of medical device development. We want to help you navigate and streamline these activities—check out our article “Why Are You Wasting Time Building Your Medical Device?” to learn more: ?? https://hubs.li/Q02NgGgx0 Heading to RAPS Convergence 2024? We'd love to connect! ?? Stop by Booth #825 and let's discuss how we can help. See you there! ?? #MedicalDevices #HealthTech #MedicalSoftware #FDA #SaMD #SoftwareDevelopment #RAPSConvergence #RegulatoryCompliance

We hear you… certain activities required by the FDA may feel like a waste of time ??, leading to frustration. However, it’s important to consider the "why" behind these, especially in the context of medical device development. We want to help you navigate and streamline these activities—check out our article “Why Are You Wasting Time Building Your Medical Device?” to learn more: ?? https://hubs.li/Q02NgGl90 Heading to RAPS Convergence 2024? We'd love to connect! ?? Stop by Booth #825 and let's discuss how we can help. See you there! ?? #MedicalDevices #HealthTech #MedicalSoftware #FDA #SaMD #SoftwareDevelopment #RAPSConvergence #RegulatoryCompliance

In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/eaRh632R

In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/e4NXKsS3