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HP0-787 NonStop Advanced Application Development

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HP0-787 exam Dumps Source : NonStop Advanced Application Development

Test Code : HP0-787
Test denomination : NonStop Advanced Application Development
Vendor denomination : HP
exam questions : 192 real Questions

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HP HP NonStop Advanced Application

Autodesk Creates Design-to-Print Workflow for HP and GE 3D Printers | killexams.com real Questions and Pass4sure dumps

Autodesk has designed an conclusion-to-end workflow that takes generative design buildings into HP Multi Jet Fusion 3D printers. Autodesk is too constructing the equal for GE Additive machines.

With original additive manufacturing machines hitting the market from HP and GE, Autodesk is ramping up generative design utility that works at once with the original printers. The company has developed a complete design-to-print workflow for additive manufacturing—in keeping with Autodesk’s Netfabb and Fusion 360—that connects Autodesk generative design technology with HP Multi Jet Fusion 3D printers.

The purpose is to streamline the conversion of digital design to actual part. The workflow is designed to boost accessibility to rapid prototyping to quicken up creation-ready 3D printed elements. Autodesk is additionally taking piece with GE Additive to create a design-to-print workflow to bring end-to-conclusion generative design to GE 3D printing machines.

3D Printing Reaches production cost

at the coronary heart of the design-to-print workflow and the HP collaboration is the build-out of construction-based mostly 3D printing that grants possible, in your expense scope additive manufacturing. “The HP multi-jet fusion printers are altering the value equation when it comes to 3D printing for production. The plastic printers at the flash are becoming cost-efficient versus injection molding for half counts in excess of 10,000 parts,” Robert Yancey, director of producing trade manner at Autodesk, told Design information. “the original steel printers promise to absorb similar cost merits in comparison to steel injection molding. HP is assisting circulation the additive manufacturing market from prototyping to creation functions.”

The shift in 3D printing construction comes from the capabilities of the brand original machines and substances. “HP multi-jet fusion printers promise larger volumes and better customization than plastic printers that absorb been available in the market for some time,” renowned Yancey. “To unlock the total expense of HP MJF printers, you requisite an excellent design, a superb material, and a fine print manner. Autodesk develops the design tools and expertise, HP develops the print process, and HP with their cloth companions develops the materials. everything aspects are required to obtain highest efficiency.”

Proving out the Workflow

Penumbra Engineering, a generative design enterprise that's a client of both Autodesk and HP, became lately enlisted by way of a shopper to design and additively manufacture a original state-of-the-artwork ultrasonic sensing gear that offers the accuracy and durability to kisser up to consume in ascetic environments. The company used Autodesk generative design and HP Jet Fusion technology to fullfil stringent performance requirements while producing a design that's light-weight and balanced ample to ensure apropos stability and ease-of-use in the box.

“The Penumbra case sight at uncovers the expense of HP working with Autodesk generative design know-how,” mentioned Yancey. “We’re aiding HP printers in Fusion 360 and Netfabb in order that HP multi-jet fusion valued clientele absorb the design and print prep tools they need. We’re working with HP to deliver assist for the original metal printers they these days introduced.”

constructing out a Workflow for GE Additive

Autodesk is additionally working with GE Additive to simplify steel additive manufacturing. The companies absorb agreed to collaborate on an integrated workflow for GE Additive machines. in keeping with the Fusion 360 platform, the workflow will connect everything phases of additive manufacturing—from design and simulation to printing methods and desktop analytics.

Autodesk is the usage of GE Additive software algorithms, interfaces, and really expert facts fashions to present predictive insights. The workflow is additionally designed to supply pervade and timeline projections within the early tiers of design in order that design engineers can design engineering and trade selections devoid of first having to physically yield the components. “Working with Autodesk will give a magnificent design-to-print environment for their purchasers, assisting lower the limitations of additive adoption whereas accelerating a consumer’s time to first decent part,” stated Lars Bruns, software chief at GE Additive in an announcement.

One-cease conclusion-to-conclusion Workflow

For GE, the intention became to strengthen a complete end-to-conclusion workflow for the GE Direct metal Laser Melting (DMLM) methods inside Fusion 360. GE and its purchasers at this time requisite to consume distinctive application products and assorted statistics codecs to proceed from conception to printed half. “The GE and Autodesk collaboration has the purpose of featuring a unique platform and atmosphere for users to conceive of a component design the usage of Fusion 360, which includes generative design,” renowned Yancey. “The platform will simulate that design, print the design, and seize everything of the valuable print facts to hold with the design file so they now absorb a unique supply of truth for every printed component.”

GE will additionally partake prefatory pervade statistics to generative design reviews so clients can evaluate pervade adaptations between the alternatives, versus simply engineering and weight variations. “this may vastly expand the expense of generative design by using giving users an environment to straight away determine both engineering and company tradeoffs for the numerous alternate options generated,” renowned Yancey.

Rob Spiegel has covered automation and manage for 17 years, 15 of them for Design information. different issues he has lined consist of provide chain expertise, altenative energy, and cyber safety. For 10 years, he was proprietor and publisher of the meals magazine Chile Pepper.


HP security Voltage's SecureData commercial enterprise: Product overview | killexams.com real Questions and Pass4sure dumps

HP acquired Voltage security in April 2015, rebranding the platform as "HP security Voltage." The product is an information encryption and key era solution that contains tokenization for shielding elegant enterprise statistics. The HP protection Voltage platform contains a lot of products, equivalent to HP SecureData business, HP SecureData Hadoop, HP SecureData payments and so forth. this text makes a speciality of HP SecureData commercial enterprise, which comprises HP format-preserving Encryption (FPE), HP comfy Stateless Tokenization (SST) technology, HP Stateless Key administration, and records protecting.

Product elements

HP SecureData commercial enterprise is a scalable product that encrypts both structured and unstructured records, tokenizes records to linger away from viewing through unauthorized users, meets PCI DSS compliance necessities, and provides analytics.

The core of HP SecureData commercial enterprise is the Voltage SecureData management Console, which gives centralized policy administration and reporting for everything Voltage SecureData techniques. a different part, the Voltage Key administration Server, manages the encryption keys. coverage-controlled utility programming interfaces permit native encryption and tokenization on various platforms, from protection assistance and adventure managers to Hadoop to cloud environments.

The platform employs a special manner called HP Stateless Key administration, which skill keys are generated on demand, based on policy stipulations, after clients are authenticated and certified. Keys will too be regenerated as essential. using stateless key management reduces administrative overhead and charges by using disposing of the captious thing hold -- there is no deserve to store, maintain song of and returned up every key it really is been issued. Plus, an administrator can hyperlink HP Stateless Key administration to an organization's identity management gadget to implement function-based mostly entry to information on the box stage.

FPE is in response to advanced Encryption commonplace. FPE encrypts information without altering the database schema, but does design minimal alterations to applications that should view cleartext information. (in many cases, most effective a unique line of code is modified.)

HP SecureData business's key administration, reporting and logging methods advocate shoppers meet compliance with PCI DSS, medical health insurance Portability and Accountability Act and Gramm-Leach-Bliley Act, in addition to state, national and European data privateness regulations.

HP SecureData trade is compatible with pretty much any category of database, including Oracle, DB2, MySQL, Sybase, Microsoft SQL and Microsoft Azure SQL, amongst others. It supports a wide selection of operating programs and structures, together with home windows, Linux, AIX, Solaris, HP-UX, HP NonStop, Stratus VOS, IBM z/OS, Amazon internet capabilities, Microsoft Azure, Teradata, Hadoop and many cloud environments.

companies that enforce HP SecureData trade can expect to absorb replete conclusion-to-end records insurance policy in 60 days or less.

Pricing and licensing

potential shoppers requisite to contact an HP revenue consultant for pricing and licensing assistance.

help

HP presents touchstone and premium advocate for everything HP safety Voltage products. common assist contains entry to the solutions portal and online assist requests, the online competencies base, electronic mail aid, enterprise hours phone support, 4-hour response time and a assist desk equipment.

premium steer comprises the equal features as touchstone support, however with 24x7 mobilephone aid and a two-hour response time.


3Qube applied sciences proclaims infni Qube Cloud Backup solution for HP NonStop programs | killexams.com real Questions and Pass4sure dumps

SAN JOSE, Calif.--(company WIRE)--At this week’s HP connect NonStop advanced Technical Boot Camp, 3Qube technologies announced infni Qube™, the first cloud backup replication and catastrophe recuperation solution for HP NonStop systems. Designed for prime availability computing environments, infni Qube offers speedy, scalable and at ease backup into a personal cloud across varied records facilities or a hybrid cloud environment.

“infni Qube is the industry’s first official, at ease, quick, scalable and incredibly accessible cloud backup automation platform for organisations with HP NonStop environments,” referred to Vinod Muthuswamy, 3Qube Chief technology Officer. “infni Qube is developed to fullfil the most difficult requirements of enterprise valued clientele, offering both the fastest records ingestion and most several cloud integration, everything at the most aggressive expense.”

infni Qube innovations reduce the consumer’s touchstone cloud backup can charge. Very rapid statistics ingestion reduces backup home windows and improves productiveness of vital entrance-conclusion components. records compression and deduplication reduce the entire footprint of facts at relaxation and facts in motion, optimizing the consumption of inner most and hybrid clouds in the again conclusion.

“closely affiliated with Tributary techniques, and leveraging their adventure and technical competencies, 3Qube makes it viable for HP NonStop and other high-availability environments to again up information locally and too securely replicate to the cloud,” said Shawn Sabanayagam, CEO of Tributary techniques, Inc.

“We bethink that HP NonStop consumers are tremendous organizations operating mission-essential applications. that's why 3Qube architected the infni Qube cloud backup retort to replicate statistics to the cloud securely, transparently and swiftly,” referred to Jimmy Mathews, 3Qube Chief revenue Officer.

For extra tips, cease via the 3Qube applied sciences sales space at this week’s HP unite NonStop advanced Technical Boot Camp.

3Qube technologies (www.3QubeTechnologies.com) allows for businesses to seamlessly “offer protection to, Scale and manage” their statistics in private and hybrid clouds. 3Qube applied sciences achieves this via patented technology, seamless integration with partner technologies, and big suffer and competencies in providing services with the optimum degree of pride.


HP0-787 NonStop Advanced Application Development

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HP0-787 exam Dumps Source : NonStop Advanced Application Development

Test Code : HP0-787
Test denomination : NonStop Advanced Application Development
Vendor denomination : HP
exam questions : 192 real Questions

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100 Automotive Advanced Driver Assistance Systems (ADAS) Companies to Watch in 2019 | killexams.com real questions and Pass4sure dumps

NEW YORK, Jan. 7, 2019 /PRNewswire/ -- Leading Sensor Suppliers to OEMs For ADAS Applications (ACC, AEB, AFL, BSM, DMS, FCW, HUD, ISA, LDW, NVS, PDS, PA, RSR, SVC) & Sensors (LIDAR, IR, SRR-MRR, LRR, Cameras (Stereo, Mono, RVC, SVC), Ultrasonic) & the Roadmap Towards Self-Driving, Driverless, & Autonomous Vehicles (AV)

Read the replete report: https://www.reportlinker.com/p05689874

- effect you requisite definitive Automotive Advanced Driver Assistance System (ADAS) competitive landscape analysis?- Succinct Automotive Advanced Driver Assistance System (ADAS) company profiles?- Evaluation IF ADAS Product Ranges & Technological insight?- Actionable trade Recommendations?

Read On To determine How This Definitive Report Can Transform Your Own Research And redeem You Time.

The emergence of the automotive advanced driver assistance systems (ADAS) market and increasing R&D spending on semi-autonomous and fully automated vehicles, has led Visiongain to publish this original report. The automotive advanced driver assistance system market is expected to brandish in the next few years because of increasing consumer require and acceptance of ADAS equipped vehicles and this is expected to feed through in the latter piece of the decade driving growth to original heights. If you want to be piece of this growing industry, then read on to determine how you can maximise your investment potential.

Report Highlights- Over 100 Tables, Charts, And Graphs- Analysis Of 100 Key Players Involved In Automotive ADAS Sensors And Applications Including- Aisin Seiki Co- Autoliv AB- Bosch Group- Continental AG- Delphi Automotive- Denso Corporation- Freescale Semiconductors- Gentex Corporation- Harman International- Hella KGaA Hueck & Co- Hyundai Mobis- Magna International Inc- Mobileye N.V- NVIDIA- Panasonic Corporation- Renesas Electronics- Takata Corporation- Texas Instruments- TRW Automotive- Valeo SA

And 80 Other Significant Companies With The Automotive ADAS Value Chain

Each Company Profile Would Generally Feature The Following- Automotive Advanced Driver Assistance Systems (ADAS) Overview- Recent Developments- Products and Service Offerings- Partnerships and Ventures- Future Outlook

Key Findings & Recommendations

Target Audience- Leading Automotive companies- Automotive OEMs- Tier 1 suppliers- Software developers- Electronics companies- Sensor specialists- Autonomous vehicle developers- AI specialists- Component suppliers- Technologists- R&D staff- NPD specialists- Consultants- Market analysts- Executives- trade development managers- Banks- Investors- Governments- Agencies- Regulators- Industry organisations

Key Questions Answered- Where should you target your trade strategy?- Which applications should you focus upon?- Which disruptive technologies should you invest in?- Which companies should you figure strategic alliances with?- Which company is likely to succeed and why?- What trade models should you adopt?- What industry trends should you be cognizant of?

Read the replete report: https://www.reportlinker.com/p05689874

About ReportlinkerReportLinker is an award-winning market research solution. Reportlinker finds and organizes the latest industry data so you acquire everything the market research you requisite - instantly, in one place.

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Stemline Therapeutics Announces Submission of European Marketing Authorization Application (MAA) for ELZONRIS™ | killexams.com real questions and Pass4sure dumps

NEW YORK, Jan. 07, 2019 (GLOBE NEWSWIRE) -- Stemline Therapeutics, Inc. (STML), a biopharmaceutical company focused on the development and commercialization of novel oncology therapeutics, announced today that it has submitted the marketing authorization application (MAA) for ELZONRIS (tagraxofusp) to the European Medicines Agency (EMA). The MAA seeks approval for treating patients with blastic plasmacytoid dendritic cell neoplasm (BPDCN). In November 2018, the EMA granted the ELZONRIS MAA accelerated assessment.

On December 21, 2018, ELZONRIS was approved by the U.S. Food and Drug Administration (FDA) for the treatment of BPDCN in adult and pediatric patients, two years and older, in both treatment-naïve and previously-treated populations. ELZONRIS is the first treatment approved for BPDCN and the first approved CD123-targeted therapy.

“The submission of the ELZONRIS MAA is another major step forward for providing this captious targeted treatment to patients, globally,” said Ivan Bergstein, M.D., CEO of Stemline Therapeutics. “We sight forward to working closely with the EMA to ensure this treatment is available to patients as quickly as possible. In parallel, their commercial team is continuing its ongoing effort to raise awareness of both CD123 testing and BPDCN worldwide. Potential European approval offers us an occasion to significantly expand the number of patients who may capitalize from ELZONRIS.”

About ELZONRIS™ELZONRIS (tagraxofusp), a CD123-directed cytotoxin, was approved by the Food and Drug Administration (FDA) on December 21, 2018 for the treatment of adult and pediatric patients, two years and older, with blastic plasmacytoid dendritic cell neoplasm (BPDCN). In November 2018, the European Medicines Agency (EMA) granted ELZONRIS accelerated assessment to the marketing authorization application (MAA), which was submitted to the EMA in January 2019. ELZONRIS is too being evaluated in additional clinical trials in other indications including chronic myelomonocytic leukemia (CMML), myelofibrosis (MF) and other CD123 positive diseases.

About BPDCNBlastic plasmacytoid dendritic cell neoplasm (BPDCN) is an aggressive hematologic malignancy with historically needy outcomes and an locality of unmet medical need. The BPDCN cell of inception is the plasmacytoid dendritic cell (pDC) precursor. BPDCN typically presents in the bone marrow and/or skin and may too involve lymph nodes and viscera. The diagnosis of BPDCN is based on the immunophenotypic diagnostic triad of CD123, CD4, and CD56. For more information, gratify visit the BPDCN disease awareness website at www.bpdcninfo.com.

About Stemline TherapeuticsStemline Therapeutics, Inc. is a biopharmaceutical company focused on the development and commercialization of novel oncology therapeutics. In December 2018, the FDA approved ELZONRIS, a targeted therapy directed to CD123, for the treatment of adult and pediatric patients, two years and older, with blastic plasmacytoid dendritic cell neoplasm (BPDCN). In November 2018, the European Medicines Agency (EMA) granted accelerated assessment to the marketing authorization application (MAA) of ELZONRIS in patients with BPDCN, which was submitted to the EMA in January 2019. ELZONRIS is too being evaluated in clinical trials in additional indications including chronic myelomonocytic leukemia (CMML), myelofibrosis (MF) and others. Other Stemline clinical candidates comprise SL-801, a novel oral wee molecule reversible inhibitor of XPO1, which is currently in a angle 1 crucible of patients with advanced solid tumors and recent data was presented at the European Society of Medical Oncology (ESMO) annual conference; and SL-701, an immunotherapeutic which has completed a angle 2 crucible in patients with second-line glioblastoma and recent data were presented at the Society for Neuro-Oncology (SNO) annual conference.

Forward-Looking StatementsSome of the statements included in this press release may be forward-looking statements that involve a number of risks and uncertainties. For those statements, they claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995. The factors that could cause their actual results to vary materially include: the success and timing of their MAA submission to the EMA CHMP; the success and timing of their clinical trials and preclinical studies for their product candidates, including site initiation, institutional review board approval, scientific review committee approval, patient accrual, safety, tolerability and efficacy data observed, and input from regulatory authorities including the risk that the FDA, EMA, or other ex-U.S. national drug authority ultimately does not agree with their data, find their data supportive of approval, or sanction any of their product candidates; the possibility that results of clinical trials are not predictive of safety and efficacy results of their product candidates in broader patient populations or of their products if approved; their plans to develop and commercialize their product candidates, including, but not limited to delays in arranging satisfactory manufacturing capabilities and establishing commercial infrastructure for ELZONRIS; product efficacy or safety concerns resulting in product recalls or regulatory action; the risk that estimates regarding the number of patients with the diseases that their products and product candidates may handle are inaccurate; their products not gaining acceptance among patients (and providers or third party payers) for inevitable indications (due to cost or otherwise); the risk that third party payors (including governmental agencies) will not reimburse for the consume of ELZONRIS at acceptable rates or at all; the company’s ability to maintain or expand sales of ELZONRIS; the company’s ability to develop and commercialize ELZONRIS; the adequacy of their pharmacovigilance and drug safety reporting processes; their available cash and investments; their ability to obtain and maintain intellectual property protection for their products and product candidates; delays, interruptions, or failures in the manufacture and supply of their products and product candidates; the performance of third-party businesses, including, but not limited to, manufacturers, clinical research organizations, clinical crucible sponsors and clinical crucible investigators; and other risk factors identified from time to time in their reports filed with the SEC. Any forward-looking statements set forth in this press release discourse only as of the date of this press release. They effect not intend to update any of these forward-looking statements to reflect events or circumstances that occur after the date hereof.

Story continues

Contact:

Investors:Stemline Therapeutics, Inc.750 Lexington AvenueEleventh FloorNew York, NY 10022Tel: 646-502-2307Email: investorrelations@stemline.com


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