Semana Nacional de Protección al Consumidor: La FDA se mantiene alerta para proteger a los consumidores de las estafas relacionadas con las vacunas contra el COVID-19

Por: Judy McMeekin, Pharm. D., comisionada asociada de Asuntos Regulatorios

In English 

SILVER SPRING, Md., 4 de marzo de 2021 /PRNewswire-HISPANIC PR WIRE/ — Se ha dicho que hay buena…

Por: Judy McMeekin, Pharm. D., comisionada asociada de Asuntos Regulatorios

In English 

SILVER SPRING, Md., 4 de marzo de 2021 /PRNewswire-HISPANIC PR WIRE/ — Se ha dicho que hay buena pesca en aguas turbulentas y ése ha sido el caso de los estafadores que buscan beneficiarse de la ansiedad y los temores asociados al COVID-19. Por consiguiente, la Administración de Alimentos y Medicamentos de los EE. UU. (FDA, por sus siglas en inglés) está al tanto de los charlatanes que buscan beneficiarse de la pandemia.

La protección de la salud de los consumidores es lo que caracteriza nuestra misión, y la FDA se mantiene alerta para proteger a los consumidores del fraude, lo que socava la confianza del público en los esfuerzos legítimos respecto a la vacuna contra el COVID-19. Aunque la distribución de la vacuna está en curso en todo el país, abundan los planes y esfuerzos deshonestos para engañar y estafar al público estadounidense.

La FDA está bien equipada para identificar y frustrar las estafas de productos médicos. La Subdivisión de Fraude de la Salud de la Oficina de Asuntos Reglamentarios, la Oficina de Investigaciones Criminales (OCI, por sus siglas en inglés) y la Oficina de Cumplimiento y Operaciones de Importación trabajan en colaboración con sus colegas en los centros de productos médicos de la FDA, la Oficina del Abogado en Jefe de la FDA y la Oficina de Salud de las Minorías del Departamento de Salud y Servicios Humanos (HHS, por sus siglas en inglés), así como con otras agencias gubernamentales como la Oficina de Aduanas y Protección de Fronteras de los EE. UU. y el Departamento de Justicia de los EE. UU.

Este esfuerzo federal unido ha permitido a la agencia minimizar el impacto del fraude en los consumidores. Por ejemplo (en inglés), los agentes de la OCI, en colaboración con las agencias asociadas, rápidamente investigaron, acusaron y obtuvieron declaraciones de culpabilidad de un hombre de Georgia y su empresa por la venta de medicamentos de marca falsificada promocionados para tratar el COVID-19. Al igual que los vendedores de aceite de serpiente de antaño, el sospechoso en este caso afirmaba que su «Inmune Shot» de $19 podía «DISMINUIR su riesgo de contraer el COVID-19 en casi un 50%». El sospechoso se enfocó en personas de 50 años o más con argumentos de venta, incluyendo declaraciones en el sitio web de la empresa tales como «Los PRÓXIMOS CINCO MINUTOS podrían salvar su vida», «… «Immune Shot» podría ser la fórmula más importante en el MUNDO en este momento debido a la nueva pandemia», «Immune Shot» no es un lujo, es una necesidad en este momento», «Simplemente, si usted se sale, usted está en riesgo», y «¿Vale su vida $19? En serio, ¿lo vale?»

En otro caso (en inglés), un agente de la OCI fue encubierto para detener a un estafador que se hacía pasar por experto en biotecnología. El sospechoso en este caso afirmaba haber elaborado una vacuna inyectable contra el COVID-19 y ofrecía inyectar a sus clientes por entre $400 y $1,000 cada uno. A principios de marzo de 2020, los agentes encubiertos de la OCI se pusieron en contacto con el sospechoso a través de mensajes en las redes sociales. El sospechoso afirmó que había elaborado y administrado vacunas contra el cáncer y el COVID-19. Alrededor de esa misma fecha, el fiscal general del estado de Washington emitió una carta de cese y desistimiento, para decirle al sospechoso que dejara de hacer afirmaciones y de ofrecer su «vacuna» contra el COVID-19. No obstante, el sospechoso indicó a los agentes encubiertos que la advertencia sólo había aumentado la demanda de sus inyecciones, que ahora él llamaba «inmunógeno» en lugar de vacuna. A pesar de haber firmado un decreto de consentimiento con el estado de Washington para dejar de vender sus supuestas vacunas, el sospechoso siguió comunicándose con el agente encubierto de la OCI y viajó a Idaho para «vacunar» al agente, donde fue detenido.

La agencia también ha encontrado productos de té que afirman ofrecer los mismos beneficios que una vacuna autorizada contra el COVID-19. Por ejemplo, la FDA emitió una carta de advertencia en enero a una empresa que vendía «Corona Destroyer Tea», que la empresa afirmaba que estaba formulado para la prevención del COVID-19. La agencia emitió otra carta de advertencia a una empresa que comercializaba un producto que, según la empresa, era una «inoculación de hierbas contra el COVID» y que formaba parte de una «investigación clínica en curso sobre su eficacia contra el COVID-19». Estos productos no probados no han sido evaluados por la FDA en cuanto a su seguridad y eficacia para la prevención o el tratamiento del COVID-19.

Los productos no probados que afirman prevenir o tratar el COVID-19, elaborados a partir de sustancias desconocidas y en condiciones desconocidas, presentan riesgos significativos para la salud del público. También pueden llevar a los consumidores a tomar decisiones sobre su estilo de vida que aumentan su riesgo de infección por el COVID-19, o a retrasar o interrumpir el tratamiento médico adecuado.

Los consumidores deben saber que las vacunas contra el COVID-19 que la FDA ha autorizado bajo la Autorización de uso de emergencia no pueden venderse en línea. Las vacunas contra el COVID-19 legítimas se distribuyen de forma gratuita. Lamentablemente, la agencia está al tanto de informes de sitios web (en inglés) no autorizados y listados en mercados en línea que supuestamente ofrecen vacunas contra el COVID-19 para la venta. Cuando la FDA encuentra dichos anuncios en línea o estos son reportados a la FDA, la agencia notifica a los mercados en línea, que entonces pueden retirar los anuncios. También tenemos conocimiento de correos electrónicos enviados a los consumidores con el logotipo de la FDA, aconsejando a los consumidores que llamen a un número de teléfono para programar una vacunación. Si los consumidores son contactados directamente por alguien que dice ser de la FDA sobre una cita para una vacuna contra el COVID-19, se trata de una estafa.

El Grupo de Trabajo dedicado a los Productos Fraudulentos relacionados con el COVID-19 de la FDA sigue vigilando el mercado, incluso en línea, en busca de productos fraudulentos del COVID-19, y la iniciativa de la Operación Quack Hack sigue aprovechándose de la experiencia de la agencia y de sus análisis avanzados, lo que ha dado lugar a la eliminación de cientos de productos ilegales del mercado. Hasta la fecha, la agencia ha descubierto cerca de 1,300 productos fraudulentos, ha enviado más de 160 cartas de advertencia (en inglés), ha emitido más de 270 quejas de abuso a registradores de dominios y ha enviado más de 290 solicitudes a varios mercados para que retiren los anuncios de productos fraudulentos del COVID-19.

La FDA seguirá trabajando con sus socios estatales y federales para tomar medidas adecuadas (en inglés) contra los malos actores que se aprovechan de las personas que buscan una vacuna contra el COVID-19 durante esta pandemia mundial. La agencia ha hecho todo lo posible para garantizar que las vacunas autorizadas disponibles para el público sean seguras y eficaces.

La FDA ha creado una serie de recursos (en español) sobre las medidas que pueden tomar los consumidores para protegerse del fraude. Además, la agencia tiene varias iniciativas de comunicación nuevas para ayudar a informar a los consumidores sobre los últimos avances médicos y científicos. Y, el 4 de marzo, la agencia participará en un chat de Twitter External Link Disclaimer en inglés (#SlamTheScam) y español (#OjoConLasEstafas) para alertar al público sobre los fraudes relacionados con el COVID-19.

La FDA necesita su ayuda para combatir el fraude y las afirmaciones engañosas. En esta «Semana Nacional de la Protección al Consumidor», alentamos a los consumidores y a los proveedores de atención médica a denunciar los sitios web y las personas sospechosas de vender productos fraudulentos o no aprobados, y no autorizados. El público puede realizar las denuncias a través de un portal en el sitio web de la FDA, que está disponible tanto en inglés como en español. Proteger a los consumidores durante el COVID-19, y en todo momento, es un pilar de nuestra misión de salud pública.

Información para los medios de comunicación: Gloria Sánchez-Contreras, 301-796-7686, gloria.sanchez-contreras@fda.hhs.gov  
Información al consumidor: 888-INFO-FDA

www.FDA.gov/Espanol

Foto – https://mma.prnewswire.com/media/1450047/COVID_19_fraud_scam.jpg

Logo – https://mma.prnewswire.com/media/317925/FDA_Logo.jpg

FUENTE U.S. Food and Drug Administration

Visure Solutions Unveils Visure Requirements ALM 6, Enabling Better Collaboration, Traceability & Performance

SAN FRANCISCO, March 4, 2021 /PRNewswire/ — As work-from-home continues to be the norm, companies and their employees must continue to adopt the use of new communication tools and platforms. For many industries, such as medical devices, automotive, and aerospace, innovative Requirements Management platforms have become increasingly important as virtual teams learn how to better collaborate. 

SAN FRANCISCO, March 4, 2021 /PRNewswire/ — As work-from-home continues to be the norm, companies and their employees must continue to adopt the use of new communication tools and platforms. For many industries, such as medical devices, automotive, and aerospace, innovative Requirements Management platforms have become increasingly important as virtual teams learn how to better collaborate. 

Today’s Requirements Management platforms must facilitate an agile approach to business, while maintaining an efficient development process. For regulated environments, this may mean even shorter times-to-market, more imaginative prioritization of business demand and, potentially, integration of design thinking processes into the development process.

One company that is leading the charge in this new Requirements Management paradigm is Visure Solutions Inc. In an effort to better support global virtual teams, the award-winning requirements Application Lifecycle Management (ALM) company has released Visure Requirements ALM 6.

For this latest version, the entire Visure Requirements ALM Platform has been redesigned to provide a state-of-the-art infrastructure that features a three-tier architecture. This new architecture uses gRPC protocol as the basis for the communication between the Visure Requirements ALM client and server, providing a faster, more reliable, scalable and secure connection.

Visure is the first in the industry to use gRPC, a modern, remote procedure call (RPC) framework that can run anywhere. The framework also connects services across languages, clouds, and data centers, and connects mobile devices to backend servers.

The protocol enables client and server applications to communicate transparently and makes it easier to build connected systems. Many companies such as Netflix and Square are already using gRPC for connecting multiple services in their environments. For Requirements Management, gRPC enables more efficiency, better traceability, higher productivity, and less room for errors.  

«Visure’s new ALM architecture is focused on providing better collaboration,» said Visure CEO Dr. Moustapha Tadlaoui. «The architecture allows the applications to be much faster and way more scalable while enabling better performance.» 

Many of Visure’s customers still use Word and Excel for Requirements Management; the new Visure Requirements ALM 6 provides them with the same user experience that Word does, but in a more user-friendly environment.

«gRPC enables us to have a desktop version with a highly scalable and performance experience,» explained Fernando Valera, Visure’s CTO. «For example, users can download a Windows app on their desktop if they want to use Word instead of the web. This gives them a flexible and more modern environment, especially when they are used to working with Word or Excel.» 

Valera said the Visure MS Office plugins are an extremely efficient way of importing requirements and traceability in the Visure Requirements ALM platform and establishing an effective round-trip in case of receiving updates in this format. In addition to the existing MS Word plugin, Visure Requirements ALM 6 incorporates a new MS Excel plugin capable of importing complex tables of requirements with attributes and traceability directly from the MS Office user interface.

The Visure Requirements ALM 6 platform also incorporates a brand-new application for authors of requirements and users who need to create items, check their statuses, establish traceability and collaborate with other users by reviewing specifications and requirements. The Visure Authoring application is a native web client that provides a simple and easy to use interface for occasional users that need a simple and streamlined interface to access and edit their information. 

Meanwhile, Visure Reviewer has been improved to take advantage of all the new usability and review features included in Visure Requirements ALM 6 platform. Visure Reviewer allows teams to collaborate, review and approve project elements.  The new platform also makes traceability easier by enabling users to generate traceability in one click.

There is a growing demand from many of Visure’s customers – who are developing highly critical systems – to have a Requirements Management tool that allows them to have lower costs, better performance, less downtime and the ability to scale, Dr. Tadlaoui said.

«There is an urgent need from our customers for this type of tool to help them boost speed-to-market while meeting compliance requirements and maintaining quality and integrity of their systems and products,» he said. «As industries and companies are trying to adapt to these changing times, Requirements ALM will remain a cornerstone for the cohesiveness of teams and the effectiveness of their processes.» 

Visure is hosting a demo webinar of the new ALM 6 Platform on March 17. Register here

About Visure Solutions

Established in 2002, Visure Solutions is a leading Requirements Management ALM company providing specialized, innovative and user-friendly solutions to implement efficient requirements management processes, aimed at guaranteeing the highest quality in the development of our clients’ products, systems and services. Visure’s all-in-one requirements management ALM platform supports requirements management, test management, bug and issue tracking, change management, risk management and variant management.

The company’s solutions are used across various industries, including aerospace and defense, automotive, banking and finance, medical devices, energy and nuclear, oil and gas, robotics and industrial automation. Visure is also a worldwide certified IREB (International Requirements Engineering Board) trainer of CPRE (Certified Professional for Requirements Engineering) by the IREB. Please visit https://visuresolutions.com/.

Media contact: Neal Leavitt, neal@leavcom.com

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SOURCE Visure Solutions, Inc.

ConvergeOne and Evolve IP Enter Strategic Hospitality Partnership

WAYNE, Pa., March 4, 2021 /PRNewswire/ — Evolve IP®, a leading international service provider of Work Anywhere™ solutions, and one of the world’s largest providers of enterprise-quality hosted communications for the hospitality industry, today announced that it has entered into a hospitality white label partnership with ConvergeOne. ConvergeOne is a proven, services led, cloud solution provider that utilizes…

WAYNE, Pa., March 4, 2021 /PRNewswire/ — Evolve IP®, a leading international service provider of Work Anywhere™ solutions, and one of the world’s largest providers of enterprise-quality hosted communications for the hospitality industry, today announced that it has entered into a hospitality white label partnership with ConvergeOne. ConvergeOne is a proven, services led, cloud solution provider that utilizes intellectual property and unique methodologies to create customer value and develop progressive solutions that connect people with purpose.

As part of the hospitality program, ConvergeOne will deliver solutions to their hospitality clients and the market in general based on Evolve IP’s solution, which is purpose-built for hotels.

Major components of the Evolve IP hospitality solution that ConvergeOne will deliver include:

  • World-class voice platform – Evolve IP’s hospitality solution is built on the world’s largest, most reliable, voice platform from Cisco
  • Guest phones – Evolve IP’s crystal-clear quality is delivered via the most advanced handsets available from Polycom, Yealink, Cisco and other hospitality phone providers. Hotels can re-use, on nearly all occasions, existing guest room phones; significantly reducing costs and easing migration to a fully hosted PBC solution.
  • Interactive room features – Guests enjoy advanced features like call accounting, superior voicemail functions, wake-up services and much more.
  • Staff calling – from the front desk to management offices to mobile phones, calls are delivered wherever staff members are, and regardless of conditions on site.
  • Contact center – fully-integrated with the Evolve IP phone system, the Evolve IP contact center solution delivers a great experience for guests and delivers key business insights and reports for hotel management.
  • Collaboration – today’s hotel groups understand the need for staff collaboration that extends from the corporate office to franchise locations. Leveraging Microsoft Teams, WebEx, and Cisco voice services, Evolve IP and ConvergeOne deliver unmatched collaboration solutions for hotel groups.

«We’re incredibly excited to be working with ConvergeOne in the hospitality market. The timing for this partnership, with the expected slowdown in the pandemic couldn’t be better,» said Paul Harrison, Managing Director for Evolve IP. «We are the experts in this industry and understand every detail that’s required to deliver a world-class guest experience.  Combining our expertise with ConvergeOne’s success in the hospitality market will enable us to expand our services into new hotel groups and venues and deliver a superior experience for their clients as life and travel returns to normal. We’re looking forward to growing our relationship and driving revenue for both of our firms.»

«Evolve IP is clearly a leading provider to the hospitality market with their ability to deliver the world’s leading VoIP platform from Cisco, plus unmatched hospitality features and Microsoft Teams integration,» said Bret Lathrop, Senior Director – Offer Management and International Alliance Practice of ConvergeOne. «While the pandemic has impacted all markets, it has hit the hospitality industry especially hard. Evolve IP and the ConvergeOne team have come up with several programs to help those businesses make an easy transition from their on-premises solution to a cloud solution; a request they have been asking for over recent years. We’re looking forward to working closely with our clients on solutions like the ones from Evolve IP has for the hospitality market.»

Why Clients Choose Evolve IP

Evolve IP enables employees to Work Anywhere™ productively and securely. Our enterprise solutions seamlessly integrate collaboration & communications, digital workspaces and contact center – all delivered from a browser on any connected device. Evolve IP’s technologies free IT to focus on business innovation, not systems and infrastructure, and enable their employees to contribute even more to the enterprise — no matter where or when they are working. Businesses that choose Evolve IP have selected a true technology partner. A company that becomes an expert extension of their IT team, an organization that listens to their needs to tailor solutions just for their business, and is responsive and engaged in every interaction.

Follow Evolve IP on Facebook, LinkedIn, Twitter and YouTube.

Photo(s):
https://www.prlog.org/12860605 

Press release distributed by PRLog

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SOURCE Evolve IP

Demos Lauds House Approval of H.R. 1

NEW YORK, March 4, 2021 /PRNewswire/ — Progressive think tank Demos issued the following statement on Thursday following the House of Representatives’ approval of H.R. 1, the For the People Act, a transformative structural reform package that will build Black and brown political power: 

«Demos celebrates the House’s approval of H.R. 1 and applauds the tireless work of organizers across the country, who have made its passage possible and moved America one step closer to being a…

NEW YORK, March 4, 2021 /PRNewswire/ — Progressive think tank Demos issued the following statement on Thursday following the House of Representatives’ approval of H.R. 1, the For the People Act, a transformative structural reform package that will build Black and brown political power: 

«Demos celebrates the House’s approval of H.R. 1 and applauds the tireless work of organizers across the country, who have made its passage possible and moved America one step closer to being a truly inclusive, multiracial democracy. By removing barriers to voting for Black and brown Americans and building the power of small donors, the For the People Act outlines a vision of what’s possible when our nation lives up to its promise of being a place where all people can lift their voices via their votes and their small dollar contributions. 

«Moving forward as a country requires us to be race-forward — both in word and in deed. At the federal level, that means passing legislation, like the For the People Act, that addresses the longstanding racial exclusions in our democracy with policy solutions proven to advance racial equity. 

«While this victory represents enormous progress, it is far from the end of our fight for a fair system. We must push for passage of the For the People Act in the Senate and for other structural reforms to our democracy, including the John Lewis Voting Rights Advancement Act, the Native American Voting Rights Act, D.C. statehood, expansion of the federal judiciary, and pro-worker labor reforms like the PRO Act and the Public Service Freedom to Negotiate Act. Demos remains committed to its work to advance our democracy as these critical pieces of legislation continue moving through Congress.»  

Media Contact:
Colleen Roache  Media@demos.org
Shanae Bass Media@demos.org
(For media interviews with K. Sabeel Rahman please contact Colleen Roache and Shanae Bass)

About Dēmos 
Dēmos is a dynamic «think-and-do» tank that powers the movement for a just, inclusive, multiracial democracy. Through cutting-edge policy research, inspiring litigation and deep relationships with grassroots organizations, Dēmos champions solutions that will create a democracy and economy rooted in racial equity.

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SOURCE Demos

Corte IDH determinará responsabilidad internacional de El Salvador por encarcelar a mujeres que sufren complicaciones de sus embarazos

Organizaciones litigantes discutirán caso que se presentara ante la Corte IDH

QUE:      

El Centro de Derechos Reproductivos y la Colectiva Feminista presentarán detalles del caso Manuela contra El Salvador que será…

Organizaciones litigantes discutirán caso que se presentara ante la Corte IDH

QUE:      

El Centro de Derechos Reproductivos y la Colectiva Feminista presentarán detalles del caso Manuela contra El Salvador que será presentado ante la Corte Interamericana de Derechos Humanos (Corte IDH) el próximo 10 y 11 de marzo. La audiencia determinara la responsabilidad internacional de El Salvador por encarcelar a mujeres que sufren complicaciones de sus embarazos.

La decisión tendrá también efectos a nivel continental pues los derechos humanos que se reconozcan allí generarán jurisprudencia que entrará a formar parte del Sistema Interamericano de Derechos Humanos el cual es reconocido por la mayor parte de países en América Latina y el Caribe.

CUANDO :     

Conferencia de prensa virtual  

Martes 9 de marzo, 2021  

10 a.m. EST/9:00 a.m. CST

Favor registrarse
*
 https://reprorights.zoom.us/webinar/register/WN_o3vOoRzfT5iqR1ehbhh0xg

 

WHO:             

– Catalina Martinez Coral, directora regional del Centro para Derechos Reproductivos

– Morena Herrera, representate de la Colectiva Feminista para el Desarrollo Local

– Pariente de Manuela

Sobre el caso:

De acuerdo con el caso, los hechos son los siguientes: Manuela era una salvadoreña de escasos recursos, vivía en una zona rural y no sabía leer ni escribir. Un día de 2008 se dirigió a evacuar a la letrina que se encontraba a unos metros de su casa porque empezó a sentir un fuerte dolor pélvico y abdominal. Ella no lo sabía, pero en ese momento tuvo una emergencia obstétrica: expulsó un feto y se desmayó, se trató de un parto precipitado a causa de su precaria salud.

Llegó al hospital, pero en vez de tratar su grave estado de salud, el personal médico la denunció por el supuesto delito de aborto, ya que creyeron que escondía una supuesta «infidelidad». La Policía la engrilletó a la camilla y la interrogó sin la presencia de un abogado.

Manuela fue indebidamente condenada a 30 años de prisión por el supuesto delito de homicidio agravado y murió en 2010, privada de la libertad y dejando huérfanos a dos hijos, porque el Estado no le brindó diagnóstico ni tratamiento apropiado para un cáncer linfático que se le desarrolló y que era la razón de los quebrantos de salud que le causaron la emergencia obstétrica.

Este litigio empezó en 2012 cuando el Centro de Derechos Reproductivos y la Colectiva Feminista presentaron el caso ante la Comisión Interamericana de Derechos Humanos. En octubre de 2019 la Comisión decidió presentar el caso ante la Corte Interamericana de Derechos Humanos considerando que el Estado salvadoreño había violado varios derechos humanos de Manuela, entre ellos, el derecho a la vida, la salud, a las protecciones y garantías judiciales, a estar libre de discriminación y violencia de género.

CONTACTO: Centro para Derechos Reproductivos; center.press@reprorights.org; WhatsApp +57 300 8284013

/PRNewswire-HISPANIC PR WIRE — 4 de marzo de 2021/

FUENTE Center for Reproductive Rights

Michelangelo’s hidden masterpiece in the heart of Tuscany, Villa Mangiacane, to Create Organic Super Tuscan Wine

Mangiacane’s compelling history dates back to the late 14th century. The villa was built by the Machiavelli family and designed by Michelangelo

FLORENCE, Italy, March 4, 2021 /PRNewswire/ — Villa Mangiacane, Michelangelo’s hidden masterpiece in the heart of Tuscany, is set to begin producing a new organic Super Tuscan wine.

<img id="prnejpg22b3left"…

Mangiacane’s compelling history dates back to the late 14th century. The villa was built by the Machiavelli family and designed by Michelangelo

FLORENCE, Italy, March 4, 2021 /PRNewswire/ — Villa Mangiacane, Michelangelo’s hidden masterpiece in the heart of Tuscany, is set to begin producing a new organic Super Tuscan wine.

Michelangelo’s Hidden Masterpiece, Villa Mangiacane

Mangiacane’s new winery director, Antonio Spurio is a student of the great enologist, Carlo Ferrini, with whom he collaborated for about 17 years.  Spurio noted that, «Besides growing Sangiovese and continuing with the great wines produced in these parts, I am convinced that this is the perfect area to create a new Super Tuscan made of Cabernet Franc. We can only anticipate that the grapes will follow a very natural vinification process, and the idea is to cultivate perfect grapes, so they do not need any additional techniques in the cellar.»

Spurio added, «The transition to organic cultivation is essential. We want to have a balance as natural as possible with the nature surrounding the estate.»

Mangiacane’s rich history dates back to the late 14th century. The villa was built by the Machiavelli family and designed by Michelangelo, the famed Italian sculpture, painter and architect of the High Renaissance. Michelangelo is considered one of the greatest artists of all time, and under the patronage of the great Medici family, he produced some of the most famous works of art in history.

Because of the historical significance of the villa’s initial owner and architect, the original building plans for improvements are housed at the world famous Uffizi Gallery in Florence. The Machiavelli family sold the villa in 1646 to the distinguished aristocratic Mazzei family who were the premium wine producers at the time and continue to be.

In 2001, the property was acquired by its current owner, who invested in a multi-million dollar renovation plan to restore the villa to its former splendor. The restoration was completed in 2007, and the villa opened its doors.

Current owner Glynn Cohen, a businessman, philanthropist and keen supporter of the arts, is known for his support of The Friends of Florence, and in particular, the renovation of Michelangelo’s The David in the Academia in Florence where there is a plaque mentioning Mangiacane.

Mr Cohen welcomed this move noting, «We will begin the conversion to organic farming immediately.  It is the only way to leave our children better land, rich in biodiversity and free of pollutants.»

Photo – https://mma.prnewswire.com/media/1450026/Villa_Mangiacane.jpg

 

 

Michelangelo’s hidden masterpiece in the heart of Tuscany, Villa Mangiacane, to Create Organic Super Tuscan Wine

FLORENCE, Italy, March 4, 2021 /PRNewswire/ — Villa Mangiacane, Michelangelo’s hidden masterpiece in the heart of Tuscany, is set to begin producing a new organic Super Tuscan wine.

FLORENCE, Italy, March 4, 2021 /PRNewswire/ — Villa Mangiacane, Michelangelo’s hidden masterpiece in the heart of Tuscany, is set to begin producing a new organic Super Tuscan wine.

Mangiacane’s new winery director, Antonio Spurio is a student of the great enologist, Carlo Ferrini, with whom he collaborated for about 17 years.  Spurio noted that, «Besides growing Sangiovese and continuing with the great wines produced in these parts, I am convinced that this is the perfect area to create a new Super Tuscan made of Cabernet Franc. We can only anticipate that the grapes will follow a very natural vinification process, and the idea is to cultivate perfect grapes, so they do not need any additional techniques in the cellar.»

Spurio added, «The transition to organic cultivation is essential. We want to have a balance as natural as possible with the nature surrounding the estate.»

Mangiacane’s rich history dates back to the late 14th century. The villa was built by the Machiavelli family and designed by Michelangelo, the famed Italian sculpture, painter and architect of the High Renaissance. Michelangelo is considered one of the greatest artists of all time, and under the patronage of the great Medici family, he produced some of the most famous works of art in history.

Because of the historical significance of the villa’s initial owner and architect, the original building plans for improvements are housed at the world famous Uffizi Gallery in Florence. The Machiavelli family sold the villa in 1646 to the distinguished aristocratic Mazzei family who were the premium wine producers at the time and continue to be.

In 2001, the property was acquired by its current owner, who invested in a multi-million dollar renovation plan to restore the villa to its former splendor. The restoration was completed in 2007, and the villa opened its doors.

Current owner Glynn Cohen, a businessman, philanthropist and keen supporter of the arts, is known for his support of The Friends of Florence, and in particular, the renovation of Michelangelo’s The David in the Academia in Florence where there is a plaque mentioning Mangiacane.

Mr Cohen welcomed this move noting, «We will begin the conversion to organic farming immediately.  It is the only way to leave our children better land, rich in biodiversity and free of pollutants.»

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SOURCE Villa Mangiacane

FASTER Act for Sesame Labeling Unanimously Passes in the Senate

MCLEAN, Va., March 4, 2021 /PRNewswire/ — Today, FARE, the world’s leading non-governmental organization engaged in food allergy advocacy and the largest private funder of food allergy research, announced that the <a target="_blank"…

MCLEAN, Va., March 4, 2021 /PRNewswire/ — Today, FARE, the world’s leading non-governmental organization engaged in food allergy advocacy and the largest private funder of food allergy research, announced that the Food Allergy Safety, Treatment, Education and Research (FASTER) Act, S. 578, was unanimously passed last night by the United States Senate. The bipartisan sesame labeling bill, which is FARE’s highest legislative priority, was introduced by Senator Tim Scott (R-SC) and Senator Chris Murphy (D-CT).

«On behalf of the nearly 1.6 million Americans who are allergic to sesame and live with the fear they could unknowingly consume this dangerous allergen, I thank Senator Scott and Senator Murphy for bringing this critical piece of bipartisan legislation forward and the entire Senate for their overwhelming support,» said Lisa Gable, chief executive officer of FARE. «We now look forward to the House of Representatives passing the FASTER Act and sending it on to the President for his signature and enacting it into law.»

The FASTER Act would require that sesame be labeled as an allergen on packaged foods. Sesame would become the ninth food allergen for which the U.S. Food and Drug Administration (FDA) requires plain-language labeling. Sesame is often used when a label reads «natural flavors» or «natural spices,» adding another layer of difficulty when consumers review product labels at their local grocery store.

The bill would also require the Secretary of Health and Human Services (HHS) to issue a report on scientific opportunities in food allergy research that examines prevention, treatment, and new cures. In addition, the legislation establishes a risk-based scientific process and framework for establishing additional allergens covered by the Federal Food, Drug, and Cosmetic Act.

«With more than 32 million Americans living with food allergies, it’s important for us to take targeted steps to address the growing challenges posed by food allergies and to protect those who are vulnerable,» said Senator Scott. «Nationwide, caring for children with food allergies costs an average of $25 billion annually and can pose extreme hardships on low- and middle-income families. I’m glad that this bipartisan legislation passed the Senate and hope that we can continue to make progress for Americans affected by this issue.»

Said Gable, «I am delighted that Senators Collins (R-ME), Gillibrand (D-NY), Tillis (R-NC), Blumenthal (D-CT), Baldwin (D-WI), Marshall (R-KS), and Warnock (D-GA) are demonstrating their support for the food allergy community as original co sponsors of this life changing legislation.»

The Senate’s passage comes a week after Congresswoman Doris Matsui (D-CA-6) and Congressman Patrick McHenry (R-NC-10) introduced the same bipartisan bill, Food Allergy Safety, Treatment, Education and Research (FASTER) Act of 2021 (H.R. 1202) in the U.S. House of Representatives.

FARE will continue meeting virtually with members of the House of Representatives to gain support for the FASTER Act and will mobilize advocates to ask that they sign on as cosponsors. The legislation will be front and center when FARE hosts its second annual advocacy event, Courage at Congress 2021: Advocate for a Cure, taking place virtually from March 8-10.

For more information on the importance of the FASTER Act, please visit foodallergy.org/faster.

About FARE
FARE (Food Allergy Research & Education) is the world’s leading non-governmental organization engaged in food allergy advocacy and the largest private funder of food allergy research. Our mission is to improve the quality of life and the health of individuals with food allergies, and to provide them hope through the promise of new treatments. FARE is transforming the future of food allergy through innovative initiatives that will lead to increased awareness, new and improved treatments and prevention strategies, effective policies and legislation and novel approaches to managing the disease. To learn more about FARE, visit our Living Teal™ YouTube channel, or www.foodallergy.org.

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SOURCE Food Allergy Research & Education

HENNESSEY TO OFFER 1000 HP UPGRADE FOR MCLAREN 765LT

SEALY, Texas, March 4, 2021 /PRNewswire/ — The Hennessey Performance Engineering (HPE) team is taking one of the quickest and fastest factory stock vehicles in the world, the 2021 McLaren 765LT, and making it even faster. This has been the mantra for John Hennessey and his team of craftsmen for the past 30 years:  If it’s fast from the factory, let’s make it faster and even more fun to drive!

SEALY, Texas, March 4, 2021 /PRNewswire/ — The Hennessey Performance Engineering (HPE) team is taking one of the quickest and fastest factory stock vehicles in the world, the 2021 McLaren 765LT, and making it even faster. This has been the mantra for John Hennessey and his team of craftsmen for the past 30 years:  If it’s fast from the factory, let’s make it faster and even more fun to drive!

«The new 765LT is underrated from the factory. We tested it on our in-house dyno and it delivered about 765 HP – at the rear wheels. This means it’s producing closer to 865 bhp in bone stock form,» said company founder & CEO, John Hennessey.  «Upgrading the 765LT to 1,000 HP will drop the 0-60 mph time to just 2.1 seconds, which is just nuts.»

The HPE1000 upgrades to the 765LT include upgraded air filters, re-mapped factory ECU calibration, stainless-steel exhaust downpipe upgrade, high-flow exhaust componentry, and chassis dyno calibration.

Cost for the HPE1000 upgrade for the McLaren 765LT is $24,950.

About Hennessey
Based in Sealy, Texas, the Hennessey business comprises Hennessey Special Vehicles, Hennessey Performance (HPE), Tuner School, and the Lonestar Motorsports Park. The company has re-engineered more than 10,000 vehicles for performance enthusiasts from around the world to deliver unparalleled driving thrills. Alongside modifying a diverse range of sports, and muscle cars since 1991, the company also applies its high-performance expertise to trucks and SUVs – and boasts its own supercar – the Venom GT.

Every Hennessey product is dyno-proven, fully track-tested, street-legal and warrantied. Customers can choose from road-ready performance-enhanced cars by Hennessey ranging from Ford and Corvette to Porsche and Lamborghini in addition to benefitting from a host of high-performance upgrades.

With its own test track, engineering curriculum for aspiring tuners, more than 50 team members and capacity to work on 40-50 vehicles at a time, Hennessey Performance is one of the world’s leading vehicle engineering companies. The new 6.6-litre V8 Venom F5 hypercar is set for customer deliveries in 2021. Boasting 1,817hp and a +300mph top speed, the company is guaranteed to deliver like never before on its mission of ‘making fast cars faster’. HennesseyPerformance.com

About John Hennessey
As the company founder and CEO, John Hennessey lives and breathes fast, fun cars. John developed a passion for pushing the limits of his cars while competing at world-renowned motorsport events including Pikes Peak, the Silver State Classic and the Bonneville Salt Flats (where he set a class world record).

What started in 1991, modifying imports out of his garage, soon morphed into building 1000-horsepower twin-turbo Dodge Vipers that gained international recognition in car magazines such as Motor Trend, Car and Driver, Top Gear, and Road and Track.

Viewed as an American icon of speed, John has achieved his vision to be the top automotive tuner and builder in the U.S. With a global sales footprint covering the U.S., Europe, Asia, South America and the Middle-East he continues to find ways to engineer greater performance from some of the world’s most iconic cars alongside the creation of the company’s own world-class hypercar.

Social media channels
YouTube: hpedesign  |  Instagram: hennesseyperformance  |  Facebook: @hennesseype  |  Twitter: @HennesseyPerf 

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SOURCE Hennessey Performance

Wounded Warrior Project Testifies Before Senate and House Veterans Affairs Committees

WASHINGTON, March 4, 2021 /PRNewswire/ — Today, Wounded Warrior Project® (WWP) CEO Lt. Gen. (Ret.) Mike Linnington testified before The House and…

WASHINGTON, March 4, 2021 /PRNewswire/ — Today, Wounded Warrior Project® (WWP) CEO Lt. Gen. (Ret.) Mike Linnington testified before The House and Senate committees on Veterans Affairs. WWP was invited to share its legislative priorities, focused on improving the long-term health and wellbeing of the wounded veterans it serves and to highlight the most pressing issues warriors face today.

WWP urges the House and Senate Committees on Veterans’ Affairs to focus on:

  • Whole health and wellness – focusing on mental health, suicide prevention, and substance use disorder.
  • Toxic exposures – granting access to care for warriors ill due to toxic exposures while in service.
  • Women veterans – access to care, military to civilian transition, and PTSD related to military sexual trauma.
  • Financial security – modernization of VA benefits and concurrent receipt for warriors injured in combat or training for combat.
  • Caregivers – mental health care for caregivers, respite care, and addressing complex care coordination challenges.
  • The Global War on Terrorism Memorial – granting authority to build the GWOT Memorial on the National Mall.

Read the entire testimony and WWP’s detailed list of recommendations for these legislative priorities.

Linnington called on the Veterans Affairs committees to implement numerous changes in policy, reforms to existing laws, and new legislation to benefit our nation’s wounded veterans living with the visible and invisible wounds of war and those struggling with their transition to civilian life.

«With the beginning of this 117th Congress, the committees have the chance to make the necessary reforms that will provide wounded veterans and their families with the resources, care, and treatment they need to thrive in their civilian lives,» Linnington said. «Our legislative recommendations, with the combined efforts of the military and veteran community, as well as our leaders in Congress and the White House, will continue to push our nation toward providing the optimal benefits veterans deserve.

Learn more about how we work with our nation’s leaders to improve the lives of wounded veterans and their families.

About Wounded Warrior Project
Since 2003, Wounded Warrior Project® (WWP) has been meeting the growing needs of warriors, their families, and caregivers — helping them achieve their highest ambition. Learn more.

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SOURCE Wounded Warrior Project