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BCP-810 Developing Applications for the(R) BlackBerry Solution

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Test Code : BCP-810
Test Name : Developing Applications for the(R) BlackBerry Solution
Vendor Name : BlackBerry
Q&A : 125 Real Questions

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U.S.: possibility for Environmental R&D cash for Small & significant organizations | Real Questions and Pass4sure dumps

On January 29th 2019,  the U.S. Strategic Environmental analysis and development program (SERDP) and the U.S. Environmental security know-how Certification software (ESTCP) launched a solicitation for each small and large corporations to competitively fund research and building for environmental research.

The department of defense (DoD) SERDP workplace is drawn to receiving white papers for analysis focusing in the areas of Environmental Restoration, Munitions Response, useful resource Conservation and Resiliency, and Weapons techniques and platforms technologies. The ESTCP workplace is drawn to receiving white papers for inventive expertise demonstrations that handle DoD environmental and installation energy requirements as candidates for funding.

SERDP helps environmental research critical to the administration and mission of the DoD and supports efforts that result in the construction and utility of ingenious environmental applied sciences or methods that increase the environmental efficiency of DoD through enhancing consequences, managing environmental risks, and/or cutting back costs or time required to get to the bottom of environmental problems.

Awardees beneath this extensive company Announcement (BAA) could be chosen through a multi-stage assessment manner. The white paper assessment step allows fascinated agencies to publish analysis white papers for govt consideration without incurring the price of a full thought. based mostly upon the white paper evaluation via SERDP, each of the white paper submitters could be notified as as to if SERDP requests or doesn't request the submission of a full inspiration. As noted in the directions located on the SERDP web page, contrast criteria for white papers are Technical benefit and SERDP Relevance.

directions within the hyperlinks beneath pertain to the submission of white papers responding to the SERDP BAA for Environmental analysis and building.  This BAA is for private Sector organizations. White papers submitted must be based on a topic listed in the guidance on this web page.

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FDA Accepts sBLA and promises priority assessment for BAVENCIO(R) (avelumab) Plus INLYTA(R) (axitinib) for the treatment of superior Renal mobile Carcinoma | Real Questions and Pass4sure dumps

food and Healthcare Press Releases วันอังคารที่ ๑๒ กุมภาพันธ์ พ.ศ. ๒๕๖๒ ๐๘:๒๕ น.

DARMSTADT, Germany and manhattan--12 Feb--PRNewswire/InfoQuest

no longer intended for US, Canada and UK-based media

Merck and Pfizer Inc. (NYSE: PFE) these days introduced that the us food and Drug Administration (FDA) has authorised for precedence overview the supplemental Biologics License utility (sBLA) for BAVENCIO(R) (avelumab) in aggregate with INLYTA(R) (axitinib)* for sufferers with advanced renal mobile carcinoma (RCC). The software has been given a target action date in June 2019.

"The combination of BAVENCIO with INLYTA builds on Pfizer's enormous heritage in advancing requirements of take care of sufferers with advanced RCC and has the potential to make a significant have an effect on for the lives of patients," referred to Chris Boshoff, M.D., Ph.D., Chief development Officer, Oncology, Pfizer global Product construction. "We appear forward to working with the FDA to bring this talents new remedy alternative to patients as straight away as possible."

"Our alliance is focused on the construction of expertise new remedy options for sufferers with cancers which have high unmet clinical wants, including the huge spectrum of people residing with advanced RCC," talked about Luciano Rossetti, M.D., govt vice chairman, Head of international analysis & building on the Biopharma business of Merck. "This regulatory milestone, which closely follows the acceptance of our software in Japan, represents a crucial step forward for science and for patients."

The submission is in accordance with statistics from the pivotal section III JAVELIN Renal a hundred and one trial, that have been offered in a Presidential Symposium at the European Society of clinical Oncology (ESMO) 2018 Congress in Munich. In December 2017, the FDA granted breakthrough therapy Designation for BAVENCIO in mixture with INLYTA for remedy-naïve patients with advanced RCC.

regardless of attainable treatment plans, the outlook for sufferers with superior RCC remains terrible.[1] approximately 20% to 30% of patients are first clinically determined at the metastatic stage.[2] The 5-12 months survival fee for sufferers with metastatic RCC is about 12%.[1]

The medical construction software for avelumab, referred to as JAVELIN, contains at the least 30 clinical programs and greater than 9,000 sufferers evaluated across greater than 15 different tumor types. apart from RCC, these tumor kinds include breast, gastric/gastro-esophageal junction, and head and neck cancers, Merkel cellphone carcinoma, non-small phone lung melanoma, and urothelial carcinoma.

*The mixture of BAVENCIO and INLYTA is beneath medical investigation for superior RCC, and there is no assure this mixture can be authorized for superior RCC with the aid of any health authority global. within the US, INLYTA is authorized as monotherapy for the treatment of superior RCC after failure of one prior systemic remedy. INLYTA is additionally accepted by means of the european drugs agency (EMA) for use in the european in adult patients with advanced RCC after failure of prior medication with SUTENT(R) (sunitinib) or a cytokine.

About Renal telephone Carcinoma

RCC is probably the most ordinary type of kidney cancer, accounting for about 2% to 3% of all cancers in adults.[3],[4] probably the most regular type of RCC is obvious telephone carcinoma, accounting for about 70% of all situations.[3] In 2019, an estimated 73,820 new cases of kidney melanoma can be clinically determined in the US.[5]

About BAVENCIO(R) (avelumab)

BAVENCIO is a human anti-programmed death ligand-1 (PD-L1) antibody. BAVENCIO has been shown in preclinical models to have interaction each the adaptive and innate immune services. by using blocking off the interplay of PD-L1 with PD-1 receptors, BAVENCIO has been proven to free up the suppression of the T telephone-mediated antitumor immune response in preclinical models.[6]-[8] BAVENCIO has also been proven to induce NK cellphone-mediated direct tumor cell lysis by the use of antibody-based cell-mediated cytotoxicity (ADCC) in vitro.[8]-[10] In November 2014, Merck and Pfizer introduced a strategic alliance to co-improve and co-commercialize BAVENCIO.

accredited signs within the US

in the US, the FDA granted accelerated acclaim for BAVENCIO for the medication of (i) adults and pediatric sufferers 12 years and older with metastatic Merkel telephone carcinoma (mMCC) and (ii) patients with locally superior or metastatic urothelial carcinoma (mUC) who have sickness progression during or following platinum-containing chemotherapy, or have sickness development within 365 days of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. These signals are authorised below accelerated approval according to tumor response price and length of response. persisted popularity of these signs can be contingent upon verification and outline of medical improvement in confirmatory trials.

BAVENCIO is at the moment accepted for patients with MCC in more than 45 nations globally, with the bulk of these approvals in a huge indication that isn't limited to a specific line of medicine.

crucial security guidance from the us FDA approved Label

The warnings and precautions for BAVENCIO encompass immune-mediated adverse reactions (corresponding to pneumonitis, hepatitis, colitis, endocrinopathies, nephritis and renal dysfunction, and different hostile reactions), infusion-related reactions and embryo-fetal toxicity.

typical adverse reactions (reported in as a minimum 20% of sufferers) in patients treated with avelumab for mMCC and sufferers with in the community superior or mUC include fatigue, musculoskeletal ache, diarrhea, nausea, infusion-connected reaction, peripheral edema, diminished appetite/hypophagia, urinary tract infection and rash.

About INLYTA(R) (axitinib)

INLYTA is an oral remedy it's designed to inhibit tyrosine kinases, together with vascular endothelial increase factor (VEGF) receptors 1, 2 and three; these receptors can affect tumor increase, vascular angiogenesis and development of cancer (the spread of tumors). within the US, INLYTA is authorized for the remedy of superior renal mobilephone carcinoma (RCC) after failure of 1 prior systemic therapy. INLYTA is additionally permitted by the eu medicines agency (EMA) to be used in the european in adult sufferers with advanced RCC after failure of prior medication with sunitinib or a cytokine.

INLYTA crucial defense advice from the us FDA permitted Label

in the analyze of advanced RCC after failure of one prior systemic therapy, the warnings and precautions for INLYTA include hypertension, including hypertensive disaster, arterial and venous thrombotic hobbies, hemorrhagic movements, cardiac failure, gastrointestinal perforation and fistula, hypothyroidism, wound healing issues, reversible posterior leukoencephalopathy syndrome (RPLS), proteinuria, liver enzyme elevation, hepatic impairment, and fetal harm during being pregnant.

regular antagonistic hobbies (reported in at the least 20% of patients) in patients receiving INLYTA have been diarrhea, hypertension, fatigue, lowered appetite, nausea, dysphonia, hand-foot syndrome, weight reduced, vomiting, asthenia, and constipation.

For more suggestions and whole Prescribing guidance, discuss with

About SUTENT(R) (sunitinib malate)

Sunitinib is a small molecule that inhibits multiple receptor tyrosine kinases, some of that are implicated in tumor growth, pathologic angiogenesis, and metastatic development of melanoma. Sunitinib become evaluated for its inhibitory recreation towards loads of kinases (>eighty kinases) and became recognized as an inhibitor of platelet-derived increase factor receptors (PDGFRα and PDGFRβ), vascular endothelial increase element receptors (VEGFR1, VEGFR2 and VEGFR3), stem cell element receptor (package), Fms-like tyrosine kinase-3 (FLT3), colony stimulating factor receptor classification 1 (CSF-1R), and the glial mobile-line derived neurotrophic component receptor (RET).

SUTENT is indicated within the US for the medicine of gastrointestinal stromal tumor (GIST) after disease development on or intolerance to imatinib mesylate; the treatment of advanced RCC; the adjuvant medicine of grownup sufferers at excessive risk of recurrent RCC following nephrectomy; and the medication of modern, well-differentiated pancreatic neuroendocrine tumors (pNET) in patients with unresectable in the neighborhood superior or metastatic ailment.

SUTENT crucial defense tips from the USA FDA approved Label

Boxed Warning/Hepatotoxicity has been accompanied in medical trials and postmarketing experience. Hepatotoxicity could be extreme, and in some cases deadly. video display hepatic feature and interrupt, in the reduction of, or discontinue dosing as counseled. fatal liver failure has been followed. display screen liver function tests before initiation of treatment, all through each and every cycle of medicine, and as clinically indicated. Interrupt SUTENT for Grade 3 or four drug-related hepatic adverse reactions and discontinue if there is no resolution. do not restart SUTENT if sufferers because of this event extreme adjustments in liver feature exams or have signals and indicators of liver failure.

further warnings and precautions for SUTENT encompass cardiovascular routine, QT prolongation and Torsades de Pointes, hypertension, hemorrhagic routine, tumor lysis syndrome (TLS), thrombotic microangiopathy (TMA), proteinuria, dermatologic toxicities including erythema multiforme, Sevens-Johnson syndrome, and toxic epidermal necrolysis, necrotizing fasciitis, thyroid dysfunction, hypoglycemia, osteonecrosis of the jaw (ONJ), impaired wound healing, embryo fetal toxicity and impaired reproductive expertise, capabilities harm right through lactation, venous thromboembolic hobbies, reversible posterior leukoencephalopathy syndrome (RPLS), and pancreatic characteristic.

regular adversarial reactions (pronounced in at the least 20% of patients) in patients receiving SUTENT for remedy-naïve metastatic RCC were diarrhea, fatigue, nausea, anorexia, altered taste, mucositis/stomatitis, ache in extremity/limb pain, vomiting, bleeding, all websites, hypertension, dyspepsia, arthralgia, stomach ache, rash, hand-foot syndrome, lower back pain, cough, asthenia, dyspnea, dermis discoloration/yellow skin, peripheral edema, headache, constipation, dry epidermis, fever, and hair colour alterations.

general opposed reactions (pronounced in as a minimum 20% of patients) in patients receiving SUTENT for adjuvant medicine of RCC, GIST or pNET - and more frequently than in sufferers given placebo - were mucositis/stomatitis/oral syndromes, diarrhea, fatigue, asthenia, hand-foot syndrome, hypertension, altered taste, nausea, dyspepsia, abdominal ache, hypothyroidism/TSH extended, rash, hair color adjustments, anorexia, epidermis discoloration, constipation, vomiting, bleeding events, epistaxis, and dysgeusia.

For more tips and whole Prescribing tips, seek advice from

About Merck-Pfizer Alliance

Immuno-oncology is a right precedence for Merck and Pfizer. The international strategic alliance between Merck and Pfizer allows the corporations to improvement from each and every different's strengths and capabilities and further explore the therapeutic competencies of avelumab, an anti-PD-L1 antibody originally discovered and developed through Merck. The immuno-oncology alliance is collectively constructing and commercializing avelumab and advancing Pfizer's PD-1 antibody. The alliance is concentrated on establishing high-priority international clinical courses to investigate avelumab as a monotherapy as well as mixture regimens, and is striving to find new how to treat melanoma.

All Merck Press Releases are distributed by means of e mail on the identical time they develop into available on the Merck web site. Please go to to register on-line, alternate your preference or discontinue this carrier.

About Merck

Merck, a leading science and expertise business, operates throughout healthcare, lifestyles science and performance materials. around 51,000 personnel work to make a positive change to millions of people's lives every day by growing more comfortable and sustainable the right way to live. From advancing gene modifying applied sciences and discovering entertaining the way to deal with probably the most challenging ailments to enabling the intelligence of contraptions - the business is everywhere. In 2017, Merck generated income of EUR 15.three billion in sixty six international locations.

Scientific exploration and in charge entrepreneurship had been key to Merck's technological and scientific advances. this is how Merck has thrived considering the fact that its founding in 1668. The founding family unit continues to be the majority owner of the publicly listed business. Merck holds the international rights to the Merck name and company. The handiest exceptions are the USA and Canada, where the business sectors of Merck function as EMD Serono in healthcare, MilliporeSigma in existence science, and EMD efficiency substances.

Pfizer Inc.: Working collectively for a more fit world(R)

At Pfizer, we observe science and our world substances to deliver therapies to americans that prolong and tremendously improve their lives. We strive to set the regular for pleasant, defense and price within the discovery, construction and manufacture of health care items. Our international portfolio contains drug treatments and vaccines as well as lots of the world's choicest-accepted consumer fitness care items. every day, Pfizer colleagues work throughout developed and emerging markets to advance wellness, prevention, remedies and treatments that challenge probably the most feared illnesses of our time. in step with our accountability as one of the crucial world's premier imaginative biopharmaceutical groups, we collaborate with health care suppliers, governments and native communities to help and expand entry to reliable, affordable health care all over the world. For more than a hundred and fifty years, we now have worked to make a difference for all who depend on us. We mechanically publish advice that could be vital to traders on our web site at in addition, to be trained extra, please consult with us on and observe us on Twitter at @Pfizer and @Pfizer_News, LinkedIn, YouTube and like us on fb at

Pfizer Disclosure notice

The suggestions contained during this unlock is as of February eleven, 2019. Pfizer assumes no obligation to replace forward-searching statements contained during this liberate as the effect of recent advice or future pursuits or tendencies.

This unencumber includes ahead-looking assistance about BAVENCIO (avelumab), together with a possible new indication for BAVENCIO in aggregate with INLYTA (axitinib) for the medicine of sufferers with advanced renal cellphone carcinoma, the alliance between Merck and Pfizer involving BAVENCIO and clinical development plans, together with their advantage merits, that contains large risks and uncertainties that might cause precise effects to vary materially from these expressed or implied with the aid of such statements. dangers and uncertainties consist of, amongst different issues, uncertainties involving the business success of BAVENCIO; the uncertainties inherent in research and development, including the ability to satisfy anticipated clinical endpoints, commencement and/or completion dates for our medical trials, regulatory submission dates, regulatory approval dates and/or launch dates, as smartly as the chance of adverse additional analyses of present scientific information and uncertainties regarding whether the other basic endpoint of JAVELIN Renal one zero one could be met; risks associated with meantime statistics; the risk that clinical trial information are discipline to differing interpretations and assessments by way of regulatory authorities; no matter if regulatory authorities might be convinced with the design of and results from our medical reviews; even if and when any drug applications may well be filed for BAVENCIO in mixture with INLYTA for the potential new indication in every other jurisdictions or in any jurisdictions for another expertise signs for BAVENCIO or mixture cures; no matter if and when the pending functions in the U.S. and Japan for BAVENCIO in aggregate with INLYTA for the potential new indication could be authorized and no matter if and when regulatory authorities in any jurisdictions where every other purposes are pending or can be submitted for BAVENCIO or aggregate healing procedures might also approve this sort of applications, so that you can rely upon myriad components, including making a decision as as to whether the product's advantages outweigh its primary dangers and determination of the product's efficacy, and, if approved, whether or not they might be commercially a hit; selections via regulatory authorities impacting labeling, manufacturing tactics and/or other concerns that may have an effect on the provision or business talents of BAVENCIO or aggregate cures, together with BAVENCIO in combination with INLYTA for the competencies new indication; and aggressive developments.

an extra description of dangers and uncertainties can be found in Pfizer's Annual document on kind 10-k for the fiscal year ended December 31, 2017, and in its subsequent reports on form 10-Q, together with in the sections thereof captioned "possibility elements" and "ahead-searching suggestions and factors That may also affect Future effects", in addition to in its subsequent studies on kind 8-ok, all of which are filed with the U.S. Securities and trade commission and available at and


1. national melanoma Institute: SEER Stat reality Sheets: Kidney and renal pelvis. obtainable from: Accessed February 2019.

2. Ljungberg B, Campbell S and Cho H. The Epidemiology of Renal mobilephone Carcinoma. Eur Urol. 2011;60:615-621.

three. American cancer Society. what's kidney melanoma? purchasable from: Accessed February 2019.

four. Escudier B, Porta C, Schmidinger M et al Renal cell carcinoma: ESMO medical apply instructions for analysis, treatment and comply with-up. Annal Oncol. 2014; 25(Suppl3):iii49-iii56.

5. American melanoma Society. melanoma records and figures 2019. purchasable at: Accessed February 2019

6. Dolan DE, Gupta S. PD-1 pathway inhibitors: changing the panorama of melanoma immunotherapy. melanoma handle. 2014;21(three):231-237.

7. Dahan R, Sega E, Engelhardt J, Selby M, Korman AJ, Ravetch JV. FcγRs modulate the anti-tumor recreation of antibodies concentrated on the PD-1/PD-L1 axis. cancer cellphone. 2015;28(3):285-295.

8. Boyerinas B, Jochems C, Fantini M, et al. Antibody-based cellular cytotoxicity exercise of a novel anti-PD-L1 antibody avelumab (MSB0010718C) on human tumor cells. melanoma Immunol Res. 2015;three(10):1148-1157.

9. Kohrt HE, Houot R, Marabelle A, et al. mixture innovations to enhance antitumor ADCC. Immunotherapy. 2012;four(5):511-527.

10. Hamilton G, Rath B. Avelumab: combining immune checkpoint inhibition and antibody-based cytotoxicity. skilled Opin Biol Ther. 2017;17(4):515-523.


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QNX Platform for Digital Cockpits brings secure Android apps to the in-car experience | real questions and Pass4sure dumps

As part of their announcements for CES 2019, BlackBerry QNX went ahead and introduced the QNX Platform for Digital Cockpits, which combines QNX Hypervisor for Safety, QNX Platform for Instrument Clusters, QNX CAR Platform for Infotainment to create a secure Android implementation for automakers to offer applications such as Google Maps and Google Play Music.

"As the ECUs in a car consolidate, automakers are seeking safe, secure, and reliable solutions that are flexible enough to deliver a unique driving experience," said John Wall, Senior Vice President and Co-Head of BlackBerry Technology Solutions, BlackBerry. "After two years of constant improvement and testing, we have built the world's first safety-certified digital cockpit that enables secure Android apps in the car. We believe being able to provide this level of security will be a key differentiator for automakers as consumers begin to weigh security and data privacy when purchasing a vehicle."

BlackBerry's QNX Platform for Digital Cockpits was built out with the help of Tata Elxsi, which BlackBerry signed a partnership with back in 2017 to design and develop secure, mission-critical solutions for automotive, industrial, medical and network communication.

"We have been enabling the Android ecosystem for mobile, Smart TV and automotive for over 10 years with our Android Center of Excellence," said Nitin Pai, Senior Vice President of Marketing and Strategy, Tata Elxsi. "The Tata Elxsi – BlackBerry partnership brings together two global and world-class companies to deliver a future-ready and yet secure digital cockpit platform with the quality and long-term support assurance that automakers seek from platform and solution providers."

QNX Platform for Digital Cockpits will make use of BlackBerry's ISO 26262 safety-certified hypervisor, which helps contain applications should they crash, be compromised or need to update. Rather than bringing down the whole system, the application will be isolated and not impact critical functions of the vehicle. If you're attending CES, you can check out the QNX Platform for Digital Cockpits demo being shown off in the 2019 Karma Revero concept car at BlackBerry's booth.

BlackBerry Empowers Automakers to Provide the Experience Drivers Want and Can Trust with the World's First Safe and Secure Digital Cockpit Solution

CES 2019 – LAS VEGAS, NEVADA – January 07, 2018 – BlackBerry Limited (NYSE: BB; TSX: BB) today unveiled the world's first digital cockpit solution that empowers automakers to provide the in-car experience drivers want, with the security, safety, and reliability they need.

The QNX Platform for Digital Cockpits enables automakers to offer a reliable and secure QNX-based digital instrument cluster and infotainment system that provides access to the latest Android-based applications such as Google Maps and Google Play Music all from a single ECU. BlackBerry's ISO 26262 safety-certified hypervisor makes sure the multiple operating system environments powering the cluster, infotainment, and other driver information systems do not interfere with one another. This isolation is important because if an app crashes, is compromised, or needs to be updated, it will not impact critical-driving functions.

BlackBerry's QNX Platform for Digital Cockpits illustrates the company's new go-to-market strategy, which is to develop and sell vertical solutions that bundle complementary products. For example, the QNX Platform for Digital Cockpits combines BlackBerry's safety-certified QNX Hypervisor for Safety, QNX Platform for Instrument Clusters, QNX CAR Platform for Infotainment, and a secure Android implementation. By delivering this cockpit solution, it will help accelerate automakers' development timelines and reduce the risk and cost of moving projects from research to production.

"As the ECUs in a car consolidate, automakers are seeking safe, secure, and reliable solutions that are flexible enough to deliver a unique driving experience," said John Wall, Senior Vice President and Co-Head of BlackBerry Technology Solutions, BlackBerry. "After two years of constant improvement and testing, we have built the world's first safety-certified digital cockpit that enables secure Android apps in the car. We believe being able to provide this level of security will be a key differentiator for automakers as consumers begin to weigh security and data privacy when purchasing a vehicle."

BlackBerry's QNX Platform for Digital Cockpits is made possible thanks to a partnership with Tata Elxsi who provide customizations and support for Android and ensure Android updates and customizations are available for the lifetime of the vehicle. The development builds on the companies' multi-year partnership, first announced in 2017, that saw Tata Elxsi sign on with BlackBerry as a value-added integrator to help companies design and develop secure, mission-critical solutions using BlackBerry QNX technologies.

"We have been enabling the Android ecosystem for mobile, Smart TV and automotive for over 10 years with our Android Center of Excellence," said Nitin Pai, Senior Vice President of Marketing and Strategy, Tata Elxsi. "The Tata Elxsi – BlackBerry partnership brings together two global and world-class companies to deliver a future-ready and yet secure digital cockpit platform with the quality and long-term support assurance that automakers seek from platform and solution providers."

BlackBerry provides OEMs around the world with state-of-the-art technology to protect hardware, software, applications, and end-to-end systems from cyberattacks. BlackBerry pedigree in safety, security, and continued innovation has led to its QNX technology being embedded in more than 120 million vehicles on the road today, as well as automotive design wins with Baidu, Delphi, Denso, NVIDIA, Qualcomm, Visteon, Jaguar Land Rover, BYTON, and more.

An early release of the QNX Platform for Digital Cockpits, in addition to other innovations, will be demonstrated in a 2019 Karma Revero concept car in BlackBerry's booth, #7523 (LVCC North Hall) at the Consumer Electronics Show (CES) in Las Vegas from January 8 - 11, 2019. The Digital Cockpit platform will also be demonstrated at the Tata Elxsi booth #815 (Tech East, Westgate) at the CES 2019.

For more information on BlackBerry's products and services for the automotive industry, please visit

About BlackBerry

BlackBerry Limited (NYSE: BB; TSX: BB) enables the Enterprise of Things by providing the technology that allows endpoints to trust one another, communicate securely, and maintain privacy. Based in Waterloo, Ontario, the company was founded in 1984 and operates globally. For more information, visit and follow @BlackBerry.

Renesas and BlackBerry Deliver R-Car Based Development Environment Integrating Virtualization, Functional Safety, and Security | real questions and Pass4sure dumps


Companies Expand Partnership To Enable Leading-Edge Automotive Systems

Renesas Electronics Corporation (6723.T), a premier supplier of advanced semiconductor solutions, and BlackBerry Limited (NYSE: BB; TSX: BB) today announced they are expanding their partnership to offer an integrated virtualization, functional safety and secure development environment for the Renesas R-Car system-on-chip (SoC) devices. Using BlackBerry’s QNX software, it was developed as part of the companies’ ongoing strategic relationship to advance autonomous and connected driving technology.

Available today, the new development environment is an expansion of Renesas’ software package lineup for the R-Car automotive computing platform. It allows automotive cockpit system designers to quickly develop advanced cockpit systems and improve the user experience.

The development environment features both the high reliability and rich graphics functions required for integrated cockpit systems. It is based on the Renesas R-Car family, and features BlackBerry's QNX Software Development Platform 7.0 and QNX Hypervisor 2.0 virtualization software. It also provides access to the extensive set of software products developed by BlackBerry, allowing designers to leverage the multimedia and HMI-related software for cockpit graphics systems development.

The development environment takes full advantage of the virtualization functions available in Renesas R-Car devices. This contributes to building functionally safe digital cockpit systems by isolating functions such as cluster and navigation, thereby ensuring that a fault in one area cannot corrupt another. The QNX Hypervisor 2.0 allows disparate guest operating systems such as Android and Linux to execute independently on a single R-Car device.

“We are very proud to build upon our long-standing relationship with Renesas to provide a leading safety-certified development environment solution for the Renesas R-Car system-on-chip (SoC) devices with BlackBerry QNX software,” said John Wall, Senior Vice President and Head of QNX at BlackBerry. “Together, BlackBerry and Renesas are enabling our customers to rapidly introduce safe and secure, high-performance cockpit systems.”

“The combination of BlackBerry and Renesas technology is used in many volume production programs globally. This speaks directly to the quality of the relationship between our companies,” said Masayasu Yoshida, Senior Director of Automotive Technical Customer Engagement Division at Renesas. “BlackBerry QNX software is always highly reliable. For Renesas, a company that strives to provide safe and secure solutions, BlackBerry is the best possible partner and we plan to continue our joint development efforts moving forward.”

The demand for highly reliable, fully integrated hardware and software is rapidly increasing in markets like China, where there is a need for the fastest possible development velocity in connected transportation. Moving forward, Renesas and BlackBerry will continue to accelerate their development of integrated cockpit systems and connected car systems, while strengthening their joint efforts for Advanced Driver Assistance Systems (ADAS) and full-scale Electronic Control Unit (ECU) integration.

About Renesas Electronics Corporation

Renesas Electronics Corporation (TSE: 6723) delivers trusted embedded design innovation with complete semiconductor solutions that enable billions of connected, intelligent devices to enhance the way people work and live—securely and safely. A global leader in microcontrollers, analog, power, SoC products and integrated platforms, Renesas provides the expertise, quality, and comprehensive solutions for a broad range of Automotive, Industrial, Home Electronics, Office Automation and Information Communication Technology applications to help shape a limitless future. Learn more at

About BlackBerry

BlackBerry is an enterprise software and services company focused on securing and managing IoT endpoints. The company does this with BlackBerry® Secure™, an end-to-end Enterprise of Things platform, comprised of its enterprise communication and collaboration software and safety-certified embedded solutions. Based in Waterloo, Ontario, the company was founded in 1984 and operates in North America, Europe, Asia, Australia, Middle East, Latin America and Africa. The Company trades under the ticker symbol “BB” on the Toronto Stock Exchange and New York Stock Exchange. For more information, visit

BlackBerry and related trademarks, names and logos are the property of BlackBerry Limited and are registered and/or used in the U.S. and countries around the world. All other marks are the property of their respective owners. BlackBerry is not responsible for any third-party products or services.

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Rohde & Schwarz Collaborates With Vector to Deliver Cellular-V2X End-To-End Application Layer Test Solution | real questions and Pass4sure dumps

WEBWIRE – Tuesday, February 19, 2019

Rohde & Schwarz has announced a collaboration with automotive E/E networking specialist Vector on a state-of-the-art cellular vehicle-to-everything (C-V2X) application layer test solution. The companies’ integrated test platform, which will be showcased for the first time at Mobile World Congress 2019 in Barcelona, combines the R&S CMW500 network simulator and the R&S SMBV100A/B GNSS simulator operating together with Vector’s CANoe .Car2x, a comprehensive software tool for simulation, development and test of V2X-based Communication Applications.


The automotive industry is evolving toward connected and autonomous vehicles that offer many benefits, such as improved safety, less traffic congestion, reduced environmental impact, and lower capital expenditure. With the trend to equip vehicles with 3GPP Release 14 C-V2X ECUs, peer-to-peer data transfer in ad-hoc networks between vehicles will be realized. All vehicles share location, speed and trajectory, enabling warnings regarding on-road dangers to be shared between drivers. Applications cover use cases such as vehicle-to-vehicle (V2V) communication, data exchange with roadway infrastructure (V2I), and interaction with vulnerable road users such as pedestrians (V2P). Data communication is implemented in the 5.8 GHz and 5.9 GHz intelligent transportation system (ITS) spectrum bands.

Rohde & Schwarz and Vector have announced the successful demonstration of a solution designed to configure and run traffic scenarios to comprehensively test the physical layer 3GPP Rel. 14 up to the application layer of C-V2X ECUs in a lab environment.

Repeatable C-V2X testing for out-of-coverage situations

Rohde & Schwarz, a leading supplier of test & measurement equipment, has expanded the capabilities of its R&S CMW500 LTE network simulator and R&S SMBV100A/B GNSS simulator to operate with Vector CANoe .Car2x, a software tool for simulation, development and test of V2X-based communication applications. The solution enables engineers to easily verify critical end-to-end safety-related V2X scenarios in a lab environment.

The solution uses the C-V2X software package for the R&S CMW500 to simulate the Physical- and MAC-layer, transmitting and receiving data over the simulated PC5 interface. This covers ideal, faded and congested channel conditions to the device under test (DUT). In its current form, the solution supports both GNSS and PSSS/SSSS sidelink synchronization options.

CANoe .Car2x offers a range of functions designed to configure and run traffic scenarios. This allows the stimulation of a C-V2X control unit according to a defined traffic situation that tests the implemented application in a structured manner. The included Car2x Scenario Editor supports the creation of traffic scenarios using a graphical interface. CANoe .Car2x generates the corresponding ITS communication based on the test scenario. The scenario is then played back with the R&S CMW500 providing the radio access layer with the specific physical interface. This verifies data transmission and reception over the PC5 interface so that the functions of the ECU can be tested comprehensively.

The combined solution covers all layers - the complete stack, 3GPP Radio Access Layers for C-V2X Mode 4, region specific ITS protocol layers such as EU ITS-G5 and U.S. WAVE and the ITS application message sets. This enables testing of specific use cases such as Emergency Electronic Brake Light (EEBL), Left-Turn Assist (LTA) or Intersection Movement Assist (IMA), as well as more complex scenarios with multiple simulated vehicles such as a congested highway. Additionally, security mechanisms could also be verified running simulations with both valid and invalid signed certificates. On top of this CANoe supports all common automotive bus connectivity such as CAN, LIN, MOST, FlexRay and Automotive Ethernet, enabling the test engineer to analyze or stimulate the ECU within an entire system from their desk. By extending the solution with the VN4610 interface from Vector, customers can access IEEE 802.11p and CAN (FD) networks as well. This enables users to analyze and test C-V2X and IEEE 802.11p (DSRC) communication and related applications with a single setup and a common user interface.

“C-V2X device testing through the application layer is a significant step towards achieving the goal of having fully connected vehicles to improve road safety,” said Anton Messmer, VP Mobile Radio Testers at Rohde & Schwarz. “Our efforts in developing and verifying C-V2X end-to-end application scenarios are enabling user equipment manufacturers and OEMs to reduce the time needed to roll out C-V2X technology on a worldwide basis.”

“CANoe .Car2x has a strong focus on testing V2X based protocols and ADAS applications. This combined solution, CANoe .Car2x with the R&S CMW500, enables our customers to stimulate the V2X ECU with real scenario data in order to perform tests from physical layer up to the application” said Stefan Krauß, Director Tools for Network and Distribution Systems at Vector. “The collaboration on this solution shows what can be achieved when leading players from the automotive and telecommunication industries work hand in hand.”

Rohde & Schwarz demonstrates the test solution at MWC 2019 in Barcelona in hall 6, booth 6C40 from 25 to 28 February 2019. For further information on C-V2X testing solutions from Rohde & Schwarz, please visit:

For further information on CANoe .Car2x, please visit:


Rohde & Schwarz

The Rohde & Schwarz technology group develops, produces and markets innovative communications, information and security products for professional users. The group’s test and measurement, broadcast and media, aerospace | defense | security, networks and cybersecurity business fields address many different industry and government-sector market segments. On June 30, 2018, Rohde & Schwarz had approximately 11,500 employees. The independent group achieved a net revenue of approximately EUR 2 billion in the 2017/2018 fiscal year (July to June). The company has its headquarters in Munich, Germany. Internationally, it has subsidiaries in more than 70 countries, with regional hubs in Asia and America.R&S® is a registered trademark of Rohde & Schwarz GmbH & Co.KG.

Vector Informatik GmbH

Simplifying the Development of Automotive ElectronicsFor 30 years, Vector has been your capable partner in the development of automotive electronics. More than 2,500 employees at 26 locations worldwide support manufacturers and suppliers of the automotive industry and related industries with a professional platform of tools, software components and services for developing embedded systems. Driven by our passion for technology we develop solutions which relieve engineers of their demanding tasks. Not only do our employees work on tomorrow’s electronic technologies every single day. We also engage variously in education, research and social responsibility.All Vector press releases are available on the internet at

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