Directory device – Annuaire 770 http://www.annuaire770.info/ Mon, 11 Oct 2021 12:34:24 +0000 en-US hourly 1 https://wordpress.org/?v=5.8 https://www.annuaire770.info/wp-content/uploads/2021/08/icon-8-150x150.png Directory device – Annuaire 770 http://www.annuaire770.info/ 32 32 Yubico Adds Fingerprint Recognition to YubiKey Hardware Security Appliance https://www.annuaire770.info/yubico-adds-fingerprint-recognition-to-yubikey-hardware-security-appliance/ Fri, 08 Oct 2021 00:37:00 +0000 https://www.annuaire770.info/yubico-adds-fingerprint-recognition-to-yubikey-hardware-security-appliance/ Today Yubico has added new biometric capabilities to its popular line of hardware security keys known as YubiKeys. The YubiKey Bio supports fingerprint recognition for use in passwordless and two-factor authentication logins. The hardware incorporates native biometric enrollment and management features that are supported by desktop services and applications and supported by FIDO. Yubico explains […]]]>

Today

Yubico has added new biometric capabilities to its popular line of hardware security keys known as YubiKeys. The YubiKey Bio supports fingerprint recognition for use in passwordless and two-factor authentication logins.

The hardware incorporates native biometric enrollment and management features that are supported by desktop services and applications and supported by FIDO.

Yubico explains that YubiKey Bio’s three-chip architecture allows biometric fingerprint material to be stored in a separate secure element that provides enhanced protection against physical attacks.

“The YubiKey Bio acts as a single, reliable root of trust, which allows the user to authenticate with the same key across multiple desktop devices, operating systems and applications,” the company says.

In addition, the YubiKey Bio enables biometric login on the desktop with all applications and services supporting FIDO protocols and works immediately with Citrix Workspace, Duo, GitHub, IBM Security Verify, Microsoft Azure Active Directory and Microsoft 365, Okta and Ping identity. With the growing adoption of modern authentication, Yubico continues to work closely with its ecosystem of partners to encourage support for biometric authentication as detailed in the WebAuthn and FIDO2 specifications.

According to Yubico CEO and co-founder Stina Ehrensvärd, the company aims to raise the bar for biometric security keys.

“[We enable] Simple and strong password-less authentication for our corporate customers and daily YubiKey users.

Chris Demundo, Senior Product Manager of Duo Security, said: “Authentication with the combined solution of the Duo platform and the YubiKey has always
was remarkably quick and easy. Biometrics play an important role in any company’s strategy to go without a password, and we have extensively tested the YubiKey Bio with Duo’s next solution, with great results. We’re excited to provide customers with an easier, faster, and more convenient way to protect themselves against phishing and other access threats.

YubiKey Bio features include:

  • Fingerprint templates stored in a separate secure item on the YubiKey Bio.
  • Support for FIDO2 / WebAuthn and FIDO U2F, based on Yubico’s invention that allows a single authenticator to operate on an unlimited number of applications, with the highest level of security and without sharing any information between services.
  • Works on desktop platforms that support WebAuthn such as Windows, macOS, Chrome OS, and Linux, and browsers such as Edge and Chrome, as well as other Chromium-based browsers.
  • Available as USB-A and USB-C in Yubico’s keychain design.
  • Portability, allowing users to switch devices, connect to shared desktops and also support mobile-restricted environments.
  • Allows the use of the security key PIN code for scenarios where biometrics cannot be used.
  • Supported by the Yubico Authenticator for Desktop app on Windows, macOS, and Linux to enroll new fingerprints, add or remove fingerprints when native platform and browser capabilities are limited.

Yubico Bio is available from retailers now.


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WhatsApp will now receive cross-device 2.0 support as well as message reactions https://www.annuaire770.info/whatsapp-will-now-receive-cross-device-2-0-support-as-well-as-message-reactions/ Wed, 06 Oct 2021 14:50:31 +0000 https://www.annuaire770.info/whatsapp-will-now-receive-cross-device-2-0-support-as-well-as-message-reactions/ Whatsapp can currently be used on up to four devices, with a smartphone. This multi-device connectivity is what allows users to sync Whatsapp to their desktops / laptops, while running the app in tandem on their smartphone. While the functionality does not extend to iPads, this should be a thing of the past as Wabetainfo […]]]>

Whatsapp can currently be used on up to four devices, with a smartphone. This multi-device connectivity is what allows users to sync Whatsapp to their desktops / laptops, while running the app in tandem on their smartphone. While the functionality does not extend to iPads, this should be a thing of the past as Wabetainfo announced that Whatsapp works on multiple 2.0 devices. The feature is already available on beta versions of the app.

What is Whatsapp Multi-Device Update 2.0?

The multi-device 2.0 update will allow users to connect to their Whatsapp accounts through different devices, without needing their smartphones to be connected to the same. This will also make Whatsapp available on the iPad.

“Multiple devices mean users will have the same features available on current public versions of WhatsApp Web, Desktop and Portal, without needing to connect your phone. Our multi-device capability immediately improves the experience for people using Desktop / Web and Portal. And it will also add support for more device types over time. Said a spokesperson.

What is Whatsapp Multi-Device Update 2.0?

What is the update of the reaction to messages from Whatsapp?

In addition to offering cross-device connectivity, Whatsapp will also introduce message reactions via its new update, according to Wabetainfo. You can long press on a message and choose from the displayed emojis how you want to react. A report on the same stated that these features are currently available in beta versions of the app.

“The reactions are not anonymous, so everyone in the conversation will be able to see who reacted to a specific message,” the report said.

Read also: Whatsapp Expands in Business Directory Market with Latest Offer

Kajoli Anand Puri

About me: Kajoli is a tech enthusiast with a soft spot for smart kitchens and home appliances. She loves exploring gadgets and gadgets designed to simplify life, but also secretly fears an AI-ruled world. Oh wait, we’re already there.
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part of modern SASE https://www.annuaire770.info/part-of-modern-sase/ Fri, 01 Oct 2021 08:06:53 +0000 https://www.annuaire770.info/part-of-modern-sase/ The roles played by API gateways and management systems are increasingly important. Whereas just a few years ago an API gateway arbitrated entry over monolithic applications within the enterprise, today’s picture is much more complex. API gateways not only handle east-west traffic between modularized applications (application compiled to DB instances to public cloud services), but […]]]>

The roles played by API gateways and management systems are increasingly important. Whereas just a few years ago an API gateway arbitrated entry over monolithic applications within the enterprise, today’s picture is much more complex.

API gateways not only handle east-west traffic between modularized applications (application compiled to DB instances to public cloud services), but APIs are an integral part of every microservice-based application. In fact, it’s safe to say that containers would currently be just a developer’s toy – just an “interesting idea” – without careful management of the data plane.

Because of the integral role APIs and their management systems play, this feature of every company’s network has a critical role to play in securing the business at large. A new generation of security brokerage systems are now commonly found at the edge of the network, acting as the canonical source of security policy for all users, devices, applications and services, wherever they are. SASE (pronounced “sassy”) may be a new buzzword, but the technology behind it isn’t necessarily new. At all levels of an SASE, from high-level security policy to data flow, API management plays a critical role in the grand scheme of zero-trust cybersecurity arrangements.

Enforcing internal API policy is as important as arbitrating inputs from outside the corporate network. This is a spread of attention that is largely aligned with the shift in cybersecurity focus from perimeter protection to a more endpoint-based set of security policies.

Because CIOs in large organizations are unlikely to be aware of the breadth of the thousands of applications used across the enterprise, even managing the basic details of keys, tokens, and access levels cannot. not be done piecemeal. The API gateway and management systems continue to play their role in the movement of data, but are increasingly important as arbiter of security in zero-trust environments.

It is therefore extremely important that API Gateway devices (or hardware device abstractions) have at least some (but preferably all) of the following.

– the ability to manage the keys or tokens of an authorization logic and to determine authorization and authentication by user, group, time, content of data flows, privilege level and location.
– offer secure self-service for entrepreneurs, developers, SREs and QA testers.
– be able to oversee and be the source of highly granular security settings for all parts of the network, i.e. be both data and control planes, or…
-… transmit these authorization parameters as dictated by other platforms, ensuring interoperability with existing security systems: an Active Directory scheme, for example simplistic.
– Support industry standard RESTful and SOAP APIs, and have the ability to tailor them if needed.
– be scalable, fast and intrinsically secure.

Here has Technical HQ, we’re looking at three API management technology vendors that can be deployed at scale and won’t introduce additional layers of complexity to manage. Likewise, the products we offer will not create bottlenecks as they represent legacy technology that has been hastily reconfigured for a microservices and multi-cloud world. In short, they are business-ready and fit-for-use platforms.

Nevatech’s Sentinet solution offers a unique ability to create authorization configurations by simply dragging and dropping from a graphical interface while creating complex, highly granular policies. For example, Sentinet access rules for managed APIs can be configured based on caller identities, message content, privilege levels, subnets, VLAN segments, API usage metrics and date / time calendars, among other variables.

Source: Shutterstock

It is also an extensible platform capable of using custom plugins which can further extend authorization with any custom logic.

At the data level, API calls can be configured to hide or show sensitive information, with full or partial logging, a critical aspect of data security compliance.

Nevatech is also unique in that its solution separates authentication schemes from specific authorization logic, allowing teams to reflect on the effect of both on overall API security.

Equally at home in the cloud as it is on-premises and available as a VM or physical hardware device, the Sentinet platform is our preferred choice for this increasingly important aspect of today’s digital businesses: their security. and their operational stability. With a self-service, customizable portal designed specifically for developers, Sentinet is the out-of-the-box API management platform of choice.

You can read more about Nevatech and the Sentinet platform here on the pages of Technical HQ, Where Click here to go to the company website for more information.

Axway’s Amplify platform is one of the company’s other offerings, ranging from simple file exchange mechanisms to automating internal APIs reminiscent of RPA functions. However, as a platform in its own right, Amplify provides businesses with a single source of information about existing API assets, no matter where they are in a distributed environment.

API

Source: Shutterstock

Any team or department that publishes API access can secure, track, and monitor its assets as part of existing or new applications and services. Conversely, consumers can use the same discovery methods to subscribe and interact with the API within the enterprise or open for external use.

At the heart of Amplify is the API Catalog, the source of detailed information about each API resource – for internal, external, SecOps, DevOps, or NetOps use, and this catalog is not a static library in read only. Instead, it adapts in real time, constantly discovering and monitoring the entire network.

To learn more about the Amplify catalog, the Amplify platform and Axway itself, click on this way to know more.

The NGINX web service platform has recently (this year – 2021) become the most used platform, overtaking the old Apache web server in number of install instances.

API

Source: Shutterstock

In addition to web service capabilities, many will know it as the benchmark platform as the world’s most trusted reverse proxy, right behind routers and firewalls around the world.

But it is in API management that NGINX is the most numerous in terms of number of installations. Much of this is due to containerized applications and services, where NGINX will arbitrate traffic between individual containers, in virtualized networks, and between discrete applications and services in the cloud – or wherever cloud-native technologies are located.

Under the guise of NGINX Plus and NGINX Controller, F5 Networks (which acquired NGINX in 2019) has successfully monetized what remains a very proud open source project, which remains free for simpler network deployments.

To learn more about NGINX’s API management capabilities in free and paid forms, Click here.

* Some of the companies featured in this article are TechHQ business partners

TechHQ


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WhatsApp begins testing in-app corporate directory, multi-device support on iOS https://www.annuaire770.info/whatsapp-begins-testing-in-app-corporate-directory-multi-device-support-on-ios/ Thu, 16 Sep 2021 07:00:00 +0000 https://www.annuaire770.info/whatsapp-begins-testing-in-app-corporate-directory-multi-device-support-on-ios/ Last updated on Sep 16, 2021, 9:03 PM WhatsApp begins testing in-app business directory, stable multi-device support on iOS app WhatsApp has two new features on the cards. First, it tests the possibility of finding local businesses or stores that offer certain products within WhatsApp itself. It could promote ad-free businesses and open up monetization […]]]>

Last updated on
Sep 16, 2021, 9:03 PM

WhatsApp begins testing in-app business directory, stable multi-device support on iOS app

WhatsApp has two new features on the cards. First, it tests the possibility of finding local businesses or stores that offer certain products within WhatsApp itself. It could promote ad-free businesses and open up monetization options for the platform.

Second, WhatsApp has rolled out multi-device support, allowing you to link your iPhone and Mac without joining the TestFlight beta program.

Here is more.

The business directory integrated into the application begins to be tested in Brazil, to remain ad-free

The Facebook-owned messaging service has started testing a feature to encourage e-commerce on WhatsApp in Sao Paulo, Brazil.

WhatsApp doesn’t allow ads on its platform, so the new feature that allows users to search for local businesses on the app could be the solution.

Reuters indicated that businesses would include categories such as food, retail and local services in certain neighborhoods.

Facebook thinks India ‘good fit’ for testing business directories

Facebook thinks India is a

Facebook vice president of commercial messaging Matt Idema said Reuters, “This could be the primary way people start a business process in WhatsApp (sic).”

Idema confirmed that the functionality could be extended to regions, including Indonesia and India. The company believes these countries are “good candidates for expanding functionality.”

Idema has hinted that WhatsApp may also introduce in-app ads on WhatsApp in the future.

WhatsApp users on stable iOS version finally get multi-device support

WhatsApp users on stable iOS version finally get multi-device support

Additionally, WhatsApp has reportedly started testing the initial version of multi-device support on Android and iOS. The feature is starting to roll out on the stable channel for iOS users.

At the moment, only four devices can be linked and none of them can be a phone except the main device. You can link macOS / Windows computers, WhatsApp web sessions, or a Facebook portal device.

Here’s how to get started with multiple devices on iOS

Here's how to get started with multiple devices on iOS

To activate the multi-device beta on iOS, update to the latest version from the App Store and select the multi-device prompt in the Linked devices section.

Joining disconnects you from current sessions. Now scan the QR code and reconnect on your devices and use them independently.

Note that you may not be able to call people using older versions of WhatsApp after this.


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Device health and telemetry management https://www.annuaire770.info/device-health-and-telemetry-management/ Wed, 15 Sep 2021 07:00:00 +0000 https://www.annuaire770.info/device-health-and-telemetry-management/ Today’s modern computing environment consists of Mac, Windows, and Linux devices, and users in many businesses are spread across the globe. All of this adds a new layer of complexity to user and device management that can easily lead to a substantial loss of productivity and / or present major security issues if not addressed […]]]>

Today’s modern computing environment consists of Mac, Windows, and Linux devices, and users in many businesses are spread across the globe. All of this adds a new layer of complexity to user and device management that can easily lead to a substantial loss of productivity and / or present major security issues if not addressed properly. This diverse IT landscape requires a modern approach to user and device management.

To keep up with current and future iterations of the modern computing environment, a device management system must recognize that users are at the heart of everything, including devices. In addition to this, the user and device management system that your organization chooses to use should include five key components and capabilities:

  1. Device health and telemetry management
  2. Management of software and operating system updates
  3. Registration and deployment without intervention
  4. Full control of user management
  5. Remote device configuration

In this article, we’ll explain why good device health and telemetry management is essential in your IT ecosystem, what types of data you need to monitor, and how to JumpCloud.® specifically addresses device health issues, whether the devices are remote or on-site with Directory and System Insights ™.

Why Modern IT Environments Need a Device Integrity and Telemetry Solution

Having a system in place that monitors devices and their overall health is critical to maintaining a secure IT environment and a productive workforce. Telemetry data pulled from devices can be used for various improvements within an organization, including (but not limited to) user experience, posture and security practices, and health and performance. applications. Health and device monitoring in this sense should not be confused with monitoring user activity and invading privacy.

With the frequency with which devices are used in an organization, likely more than 40 hours per week, problems can arise if these devices are not managed and not closely monitored for updates, security breaches and inconsistencies. Whether you have a device management system already in place or if you are looking to implement one from scratch, you should take into account the health data of the device you are currently using (Read more…)


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JumpCloud Raises $ 159 Million to Help Manage Users and Devices https://www.annuaire770.info/jumpcloud-raises-159-million-to-help-manage-users-and-devices/ Mon, 13 Sep 2021 07:00:00 +0000 https://www.annuaire770.info/jumpcloud-raises-159-million-to-help-manage-users-and-devices/ JumpCloud has closed its Series F cycle and posted a valuation of $ 2.56 billion to add additional capacity to its directory platform and drive sales from its channels. The Louisville, Colo.-Based company plans to use the money to expand its cloud directory platform beyond basic identity features like single sign-on, device management, l ‘multi-factor […]]]>

JumpCloud has closed its Series F cycle and posted a valuation of $ 2.56 billion to add additional capacity to its directory platform and drive sales from its channels.

The Louisville, Colo.-Based company plans to use the money to expand its cloud directory platform beyond basic identity features like single sign-on, device management, l ‘multi-factor authentication, identity governance and administration and privileged access management, according to the CEO. Rajat Bhargava. JumpCloud also wants to leverage its base of more than 1,200 MSP partners to reach more SMB customers.

“There is such a great opportunity for our channel partners to shift away from a device-centric model to a user-centric model,” Bhargava told CRN. JumpCloud’s $ 159 million funding round was led by venture capital firm Sapphire Ventures and comes just eight months after the company completed a $ 100 million Series E funding round led by BlackRock Innovation Capital.

[Related: Identity Firm JumpCloud Raises $75M To Boost Ties With MSPs]

JumpCloud now makes between 15-20% of its sales through the channel, and Bhargava said he would like to see about half of the company’s business go through long-term solution providers. The company mainly sells to customers with between 50 and 5,000 seats, and those without an internal IT function almost always prefer to source their products through an MSP, he said.

The company has invested in features like a multi-tenant portal that make it easier for MSPs to manage their JumpCloud customers, Bhargava said. JumpCloud plans to use the F-Series funding to invest in more technical and sales staff for solution providers as well as marketing resources around content and partner activation, Bhargava said. The company has customers in more than 100 countries, he said.

“For us to be successful in this market, we basically have to be very close to PSMs,” Bhargava said.

From a technology perspective, Bhargava said that JumpCloud is looking to invest in capabilities that allow users to easily and securely access the computing resources they need both on-premises and in the cloud. Although JumpCloud has not made any acquisitions since its founding nine years ago, Bhargava expects mergers and acquisitions to be part of the company’s feature expansion strategy going forward.

“The cloud-based directory platform that we are building will encompass all of those ancillary categories that existed as point solutions that organizations had to purchase in addition to [Microsoft] Active Directory, ”Bhargava said. “We are trying to [consolidate] this stack of solutions in one platform.

One of the main advantages of JumpCloud over its directory service competitors is that it can support Windows, Mac, and Linux deployments in both the cloud or on-premises, as well as Google Workspace, Microsoft 365 and Amazon Web Services collaboration. JumpCloud also secures connections to devices and servers rather than focusing only on connections to web applications, he said.

From a metrics perspective, Bhargava said JumpCloud primarily focuses on annual recurring revenue growth (ARR) as well as net revenue retention (NRR). NRR reports whether customers like JumpCloud’s product and see the company as a long-term partner in following their growth with the company, according to Bhargava.

“Over the years, we have had an incredible chance to build a great business and we want to continue to do so,” Bhargava said. “Being able to get that kind of information out will hopefully send the message that we’re here for the long haul.”

Macktez started using JumpCloud five years ago to perform RADIUS authentication against Google Apps, and was impressed with the company’s ability to work across multiple operating systems and in remote-centric environments, said technical director Reilly Schull. JumpCloud has everything from authenticating local devices and managing mobile devices to managing encryption keys and syncing passwords, he said.

Because of its integrations, Schull said Macktez customers see the exact same JumpCloud start page whether they sign in to Microsoft, Google, or Apple.

“It’s an extremely unified experience with an extremely useful feature set,” said Schull.

Going forward, Schull said he would like to see JumpCloud increase its lead in mobile device management and develop increased integrations with Microsoft to bring group management to the same level as for Google and Amazon. As JumpCloud moves upmarket, Schull said he will meet more customers using Microsoft services, making increased collaboration with Microsoft critical in the long run.

“If people aren’t familiar with JumpCloud, they really should try it,” Schull said. “It’s a very good product.”


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Expected lifespan of medical devices at a glance https://www.annuaire770.info/expected-lifespan-of-medical-devices-at-a-glance/ Wed, 08 Sep 2021 07:00:00 +0000 https://www.annuaire770.info/expected-lifespan-of-medical-devices-at-a-glance/ The life expectancy of medical devices is currently a hot topic in the industry, given the requirement of the European Medical Device Regulation, EU MDR 2017/745, Article 18 1 (c). Article 83 Post-market surveillance, Article 86 Periodic safety update report, Annex XIV part B – Post-market clinical monitoring is also linked to the expected lifespan […]]]>

The life expectancy of medical devices is currently a hot topic in the industry, given the requirement of the European Medical Device Regulation, EU MDR 2017/745, Article 18 1 (c). Article 83 Post-market surveillance, Article 86 Periodic safety update report, Annex XIV part B – Post-market clinical monitoring is also linked to the expected lifespan of the device. Manufacturers are required to provide a defined expected life for certification of their product under the new European medical device regulations. There has been a lot of discussion about how best to define the expected lifespan of the device and what to consider when defining it.

Define the “expected lifespan” of a medical device

Let’s take a look at the definition of expected device life. “This is a period during which the device is intended to perform its function in accordance with the risk and benefit profile of a medical device, and to maintain its benefits without adding additional risk to the patient. Overall, the expected life of the medical device can match the intended use, as specified in the considerations listed below (MedTech Europe Paper).

Consideration 1: The lifespan of devices intended to be used only for a specific period (i.e. catheters for deploying a stent) is defined by their duration of use.

Consideration 2: The lifespan of devices intended to entirely replace a bodily function (i.e. a joint in the human body) would be ideal for the remainder of the patient’s life. It is recognized that advanced devices for the intended use may have a limited lifespan and may need to be removed / replaced depending on physician monitoring and evaluation.

Consideration 3: The lifespan of devices intended to function in the body for a limited period of time (i.e. absorbable implants) is defined by their therapeutic lifespan, their function plus the time remaining until absorption. in the human body.

Consideration 4: The lifespan of devices which have a temporary function in the human body (i.e. implants for bone healing or nonabsorbable sutures), is defined by their function in the human body up to the point of withdrawal.

Each consideration listed above could include many elements, which are explained in this article. It is essential to understand that the lifespan of a medical device may or may not be based on a single element. Instead, it is a combination of several characteristics to carefully identify the safe duration. Items include patient outcomes, product design, clinical utility, observed product performance, benefits and risks including positive / negative impact on clinical outcome, patient quality of life , diagnostic outcomes and the positive / negative implications of diagnostic devices on clinical outcomes. There are external factors that could contribute such as patient anatomy, disease progression. Depending on the extent of the external factors, there may not be a specific duration based on bench testing; therefore, for advanced medical devices, manufacturers must consider the actual factors and provide the necessary instructions afterwards to establish safe performance.

First, it is imperative to understand the medical device within its scope, which will dictate which elements will apply and align the result accordingly. To begin with, it is necessary to first identify the primary element, which defines at a high level the overall function of the device in the body, followed by secondary supporting elements such as residual risk. Not all items apply to the affected device type. Let’s dive a little deeper into each of these and understand the correlation with device life.

  1. Reliability / durability tests:

Reliability testing is an essential element that resonates directly in defining the lifespan of devices. Reliability testing is the length of time a device is tested over multiple cycles or periods of use of the medical device, based on actual testing of the medical device. Review bench testing verification and durability tests performed against the relevant standards to assess the performance of the respective medical device to ensure that the design of the product / system will meet the user’s needs, taking into account the environment of use (in vitro data).

Fatigue tests are performed as a measure of reliability and durability. It is the process of gradual application of a cyclic loading leading to a permanent structural change occurring in a material subjected to relevant conditions which produce fluctuating stresses and strains at certain points and can affect the product after a sufficient number cycles / fluctuations. It is not necessary to have an infinite number of cycles to cause structural damage, on the contrary, it will be based on the recommended standards for the type of classification and use of the device.

  1. Clinical performance:

The clinical performance attributes define the clinical significance of the device and provide clinical results confirming the bench test results. It includes confirmation of support for device performance attributes, patient outcomes, etc. Depending on the classification of the device, the clinical performance validates the bench tests and confirms the expected lifespan of the medical device.

To assess the performance and safety of the device through clinical literature, investigations, preclinical evaluations, ongoing studies, etc., for the intended clinical use of the device.

  1. Residual risk:

(Note: for implantable devices, the residual risk that results from the entire period of residence of the device inside the patient’s body):

The risk management process involves the assessment of residual risk over the life of the product. The benefits are compared to the residual risks to ensure that the acceptability of the risk is justified. Refer to details on risk assessment and conclusion of acceptability of benefit / risk for this product.

When determining the appropriate expected life of the device, it is important to determine whether certain hazards are introduced for certain phases of the potential life of the product and whether those hazards are acceptable or appropriate to discontinue use. of the product in order to avoid risks. The risk considerations for the expected life of the device for this product are described below.

Example: This product has been tested for reliability performance over five years. Beyond five years, the potential for increased residual risk due to product failures has been taken into account; however, this risk is considered acceptable due to the monitoring of product performance and the associated corrective action process, which can be used to deal with unexpected increases in patient risk.

Clinical evaluation: The decision to use a medical device as part of a clinical procedure requires weighing the residual risks against the expected benefits of the procedure. Explain the clinical performance and benefits of the device, when to use it and why it outweighs the risks. Evaluate the performance attributes of the medical device assert its integrity; use clinical studies to supplement the rationale.

Also assess whether characteristics related to the degradation of clinical performance of a medical device may cause unacceptable risk to essential performance.

Post-market surveillance: If applicable and available, use post-market surveillance information to document how observed performance falls within expected performance defined in the risk management plan / report. If any indicators have been observed during the product’s commercial history or any significant or critical risk currently present in the field, provide a thorough assessment of why the risk is acceptable over the expected life of the device.

  1. Shelf life / expiration date of the medical device:

Shelf life is typically used to define the expected lifespan of a single-use device. Shelf life is the length or established period of time that a product remains fit for its intended use, as demonstrated by objective evidence. Product shelf life dictates how long you can expect a product to maintain expected safety and performance, measured from the date of manufacture to a validated end point. This duration varies depending on the type of product, its use and storage. Depending on the use of the device, the shelf life may represent the expected life of a medical device or provide the life of a device to function as intended. Additional information is provided below for consideration of the shelf life determination.

Note: The shelf life / expiration date refers to the expiration date. If the device includes an implant, the life of the implant should not be confused with the expiration date of the entire device.

Material degradation: An expiration date is the end of the shelf life, after which a medical device may no longer perform as expected. Degradation or anticipated degradation is the established time period after which the product or component is expected to decline in quality or effectiveness. To determine if a device requires an expiration date, several different parameters need to be considered. The device should be analyzed to determine whether it is susceptible to degradation that would result in functional failure and the level of risk the failure would present. Evaluate whether the medical device concerned depends on certain characteristics of the component or on the expiration date; this assessment is used to determine the overall expected lifespan of the medical device.

Package stability: The stability of packaging material is the extent to which a product it contains remains as is, within specified limits, and throughout its period of storage and use. This is the established period during which the product has been validated to meet all predetermined requirements for design, quality and effectiveness.

Guarantee of sterility: The assurance of sterility is a crucial element in determining the safety of a medical device. Sterility must be maintained throughout the period of transport, storage and use. The level of cleaning and disinfection required depends on the use of the device. All reusable devices must be able to clean to a certain level, and this level depends on the risk of the device. Single-use devices must maintain the level of sterility for the expected life of the device. Depending on the use of the device, the sterility of the device could impact the expected safe use of the device, thus defining the shelf life.


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Families Affected by Autism Can Request a Free Amazon Device https://www.annuaire770.info/families-affected-by-autism-can-request-a-free-amazon-device/ Wed, 08 Sep 2021 07:00:00 +0000 https://www.annuaire770.info/families-affected-by-autism-can-request-a-free-amazon-device/ Bids will be open throughout the month or until all devices have been awarded. Families in the region affected by autism have the opportunity to receive an Amazon Echo Show 5 device through the Autism Society of Mahoning Valley. State Farm agent Shannan Jursa donated 200 devices to help people ages 12 and older with […]]]>

Bids will be open throughout the month or until all devices have been awarded.

Families in the region affected by autism have the opportunity to receive an Amazon Echo Show 5 device through the Autism Society of Mahoning Valley.

State Farm agent Shannan Jursa donated 200 devices to help people ages 12 and older with executive function and life skills needs.

Families can request a device here. Bids will be open throughout the month or until all devices have been awarded.

“Giving back to neighborhoods is what State Farm does all year round with grants, volunteerism and outreach programs like this,” Jursa, longtime ASMV volunteer, said in a statement. Press. “We live in these communities and understand the struggles of the autistic population in the Mahoning Valley and beyond.”

The donation is part of State Farm’s Diversity and Inclusion in the Community program.

“We are very grateful to Shannan for wanting to help our families. Echo Show 5 can help people with autism increase their social skills and develop more independence, ”Robin Suzelis, director of ASMV, said in the statement. “Making to-do lists for school, learning how to use the integrated grocery list, setting alarms for school or work transition is very helpful. Moreover, they can also stream podcasts or play audiobooks to improve leisure and school time. “


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Study: Seattle startup blood self-collection device accurate for COVID-19 antibody samples https://www.annuaire770.info/study-seattle-startup-blood-self-collection-device-accurate-for-covid-19-antibody-samples/ Tue, 07 Sep 2021 07:00:00 +0000 https://www.annuaire770.info/study-seattle-startup-blood-self-collection-device-accurate-for-covid-19-antibody-samples/ Tasso-SST device for self-collection of blood. (Photo of the Cup) Self-administered device for collecting blood produces high-quality antibody samples and works successfully in a high proportion of users, according to a study of people who have previously been infected with COVID-19 led by researchers from Seattle. The experimental device, made by the Seattle-based startup Cup, […]]]>
Tasso-SST device for self-collection of blood. (Photo of the Cup)

Self-administered device for collecting blood produces high-quality antibody samples and works successfully in a high proportion of users, according to a study of people who have previously been infected with COVID-19 led by researchers from Seattle.

The experimental device, made by the Seattle-based startup Cup, has the potential to supplant some of the blood tests normally taken from a vein in the clinic.

The Tasso-SST device works on the upper arm, drawing blood from a network of capillaries under the skin. The patient presses a button on the device, which pierces the skin with a spring-loaded lancet and creates a vacuum to help collect the blood.

Researchers at Tasso, the University of Washington, and the Fred Hutchinson Cancer Research Center tested the device in 99 study participants. One group had recovered from a previous COVID-19 and must have had antibodies to the virus, and a second group had no history of the disease.

The test was designed to ask if patients are producing enough antibodies against the virus to donate them to people with ongoing infections. The self-collected samples were compared with samples taken with the device under surveillance and with blood drawn from a vein by a phlebotomist.

Antibody results for each participant were similar among all samples, the researchers found. This is even if the Tasso-ST samples were subjected to conditions mimicking the 48 hour shipment, compared to the immediate processing of the samples taken by the phlebotomist.

“There was an almost perfect correlation between the venous blood results and the capillary blood samples,” lead author Chihiro Morishima said in a UW Press release. “The results were as good as we could have hoped,” added Morishima, associate professor of laboratory medicine and pathology.

The results are in line with previous research showing that antibodies tend to be stable in blood samples.

Although the samples were in good condition, some participants had to use the device twice to get enough blood. Eighty-five participants (93.4%) generated enough blood for analysis on their first attempt, compared to 90 participants (98.9%) with a successful blood draw from a vein. Almost all of the participants had at least some college education.

The device is designed to collect more blood than the average finger prick, which averages about 1/3 milliliter in the study. This is sufficient for the manual analysis performed in the study, although automated instruments may require more.

Further studies with Tasso-SST remain ongoing, including another COVID-19 antibody study funded by Fred Hutch partly by Amazon. Tasso VP of the product Nick end is also a former senior director of product management at Amazon.

Last July, the 9-year-old company raised $ 17 million in addition to the $ 13.1 million Funding Defense Advanced Research Projects Agency (DARPA), Defense Threat Reduction Agency (DTRA) and National Institute of Health (NIH).

Tasso also markets a self-collection device for storing and transporting small, dried blood samples as dots on a strip. This device authorization received this May in the European Union for non-diagnostic uses, such as monitoring blood component levels during clinical trials. This device uses technology similar to that of the Tasso-SST.

As more studies emerge demonstrating the utility of serology in the management of COVID-19, “we believe the FDA will recognize the clinical diagnostic value of these tests and open up avenues for clearance,” said Tasso CTO Erwin Berthier in an email to GeekWire. He co-founded the company with a colleague bio-engineer and CEO Ben Casavant in 2011.

Tasso funded the new study, participated in the research, and approved the final manuscript. The company was not involved in decisions on how to analyze or present the data, according to PLOS One, which released study.


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JumpCloud expands leadership rankings for Identity, Device, https://www.annuaire770.info/jumpcloud-expands-leadership-rankings-for-identity-device/ Tue, 07 Sep 2021 07:00:00 +0000 https://www.annuaire770.info/jumpcloud-expands-leadership-rankings-for-identity-device/ LOUISVILLE, Colorado, September 7, 2021 (GLOBE NEWSWIRE) – Cloud directory platform provider JumpCloud announced today that it has been named a leader in several categories of identities, devices and directories by G2, the industry’s most trusted source for customer reviews. JumpCloud continues to expand its leadership in a number of categories based on over 800 […]]]>

LOUISVILLE, Colorado, September 7, 2021 (GLOBE NEWSWIRE) – Cloud directory platform provider JumpCloud announced today that it has been named a leader in several categories of identities, devices and directories by G2, the industry’s most trusted source for customer reviews. JumpCloud continues to expand its leadership in a number of categories based on over 800 reviews and ratings of verified G2 users. Continuous innovation and product expansion have helped JumpCloud extend and maintain its leadership position in the Grid for Cloud Directory Services report for the past four reviews – one of the only vendors to consistently hold a position leader since the report was first published.

“Rather than tinkering around with narrow and expensive point solutions, IT administrators are finding that JumpCloud’s modern directory platform better and more securely supports their organization’s IT needs with flexibility, convenience and cost savings,” said Rajat Bhargava, CEO of JumpCloud.

JumpCloud has been named a Leader in the following 13 Grid Reports:

Category: Single sign-on (SSO)

  • Small-Business Grid® Report for Single Sign-On (SSO) | Fall 2021
  • Mid-Market Grid® Report for Single Sign-On (SSO) | Fall 2021
  • Grid® Report for Single Sign-On (SSO) | Fall 2021
  • Momentum Grid® Report for Single Sign-On (SSO) | Fall 2021
  • Europe Regional Grid® Report for Single Sign-On (SSO) | Fall 2021

Category: User provisioning and governance tools

  • Grid® Report for Provisioning and User Governance Tools | Fall 2021
  • Momentum Grid® Report for Provisioning and User Governance Tools | Fall 2021

Category: Identity and Access Management (IAM)

  • Grid® Report for Identity and Access Management (IAM) | Fall 2021
  • Momentum Grid® Report for Identity and Access Management (IAM) | Fall 2021

Category: Privileged Access Management (PAM)

  • Grid® Report for Privileged Access Management (PAM) | Fall 2021
  • Momentum Grid® Report for Privileged Access Management (PAM) | Fall 2021

Category: Cloud directory services

  • Grid® Report for Cloud Directory Services | Fall 2021
  • Momentum Grid® Report for Cloud Directory Services | Fall 2021

G2 Grid reports are released quarterly and rank products based on reviews collected directly from its user community, as well as aggregated data from online sources and social media. Products named in the Leader quadrant are “well rated by G2 users and have substantial market presence scores”.

JumpCloud has solidified its leadership in the industry by approaching user identity from a holistic perspective. Building on its foundation as a cloud directory, JumpCloud’s platform includes single sign-on, mobile device management (MDM), multi-factor authentication (MFA), PAM, and more. Capable of supporting heterogeneous device environments and managing on-premise and cloud-based applications and services, JumpCloud gives administrators a single tool to secure users and their devices, wherever work takes place.

“I can’t say there’s anything I don’t like about JumpCloud,” said Todd Hughes, IT support at Powerchord Systems, in a G2 exam. “Their customer service was there for us whenever we had questions. They have always been able to point us in the right direction to solve problems. They make our operations smoother, giving me time to focus on other important issues. We are able to manage our devices and users with ease. Our company is also taking advantage of the ability to use JumpCloud as an inventory tool. The ability to configure device policies is impressive. The only major advantage that we have achieved is the saving of time. Being able to use one app to do so many different things has been the most beneficial aspect of our business. We are able to install software from the command line in an instant.

Over 100,000 organizations worldwide use JumpCloud to securely connect users to all the computing resources they might need. To try the JumpCloud Directory Platform, forever free for up to 10 users, sign up here.

About JumpCloud

JumpCloud’s mission is to Make Work Happen®, providing people with secure access to the resources they need to do their jobs. The JumpCloud Directory Platform provides IT, Security Operations, and DevOps a single, cloud-based solution to control and manage employee identities, their devices, and apply Zero Trust principles. JumpCloud has a global user base of more than 100,000 organizations, with more than 3,700 customers, including Cars.com, GoFundMe, Grab, ClassPass, Uplight, Beyond Finance and Foursquare. JumpCloud® is supported by BlackRock, General Atlantic, OpenView, HIG Capital and Foundry Group.

        


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