Business Wire

Centerity Recognized for Market-Leading AIOps Platform with Integrated Cyber Security

Share

Centerity Systems, Inc., the leading AIOps Platform with advanced performance analytics and integrated security, today announced its recognition as a Top Value Leader in the latest “EMA Radar Report: AIOps – A Guide for Investing in Innovation.”

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201022005664/en/

To view this piece of content from mms.businesswire.com, please give your consent at the top of this page.

EMA recognizes Centerity for market-leading AIOps platform with integrated security (Graphic: Business Wire)

EMA evaluated 17 AIOps vendors on (i) Business Impact and IT-to-Business Alignment, (ii) Incident, Performance, and Availability Management, and (iii) Change Impact and Capacity Optimization use cases to guide organizations with their AIOps platform selection. Centerity’s AIOps Platform is designated as a market leader in all of the use cases EMA evaluated. Centerity is a front-runner in delivering exceptional value in both the Business Impact and IT-to-Business Alignment and Incident, Performance, and Availability Management use cases, due to its technical strength, impact on business outcomes, and deployment cost efficiency. In addition, Centerity was honored by EMA with a special award for advanced integrated security functionality.

The Centerity AIOps Platform improves performance and reliability of business and operational processes, employing an approach that continuously measures the overall health of key technology services by providing real-time, consolidated business analytics. SLA executive dashboards expose business and security risks, identify performance anomalies, and provide fault isolation across applications, operating systems, infrastructure and cloud assets. It does this by automating topology and dependency maps of all IT assets, incorporating each asset into business and operational service views. Its AI-driven anomaly detection and multi-tenancy supports multi-user, multi-vendor, and multi-location management, which is ideal for managed service providers, cloud service providers, and enterprises.

“Centerity is a unique innovator in the AIOps arena,” said Dennis Drogseth, EMA vice president. “Centerity stands out for its advancing use of AI/ML in a variety of contexts, including ‘CyberOps,’ as well as its distinctive strengths in discovery across domains, data assimilation, and unifying views and dashboards. These strengths, along with the platform’s fast time to value and limited administrative overhead all help to make Centerity both a versatile and progressive choice for AIOps adopters.” According to EMA’s evaluation, the Centerity AIOps platform is differentiated among its competitors by:

  • Delivering many of the benefits of larger and more costly AIOps suites with reduced administrative overhead and more modest software costs.

  • Bringing the full seven-layer stack together with an eye toward IT service performance and business outcomes and priorities across cloud, hybrid, and legacy environments.

  • Integrating artificial intelligence and machine learning capabilities to support security and risk management needs – such as cybersecurity compliance, endpoint detection and response (EDR), supply chain security, and automated prevention of attacks on network hardware.

According to EMA, the message for IT organizations looking to pursue a forward path in AIOps adoption is overall a strongly positive one. The benefits achieved are growing in diversity and value. AIOps can and should be transformative in enabling more effective decision-making, data sharing, and analytics-driven automation. The recommendation from EMA remains that buyers should consider their own realities, then begin a search for the AIOps platform that most fits their requirements.

“In the digital age, AIOps, security and risk management must be observed and correlated through a single platform,” said Roi Keren, CEO of Centerity Systems. “That’s not only what we see our customers need and want, it’s what Centerity does best. EMA’s positioning of Centerity and award for integrated security acknowledges the convergence of AIOps and security. It’s more critical than ever for enterprise executives – whether you’re a CIO, CISO, CEO, or board member -- to make strategic, risk-based business decisions with one platform, one dashboard; in essence, a single source of truth.”

AIOps Deployments and the Real Word: Bringing Operations and Security Together

Enterprises can see how others are deploying AIOps to address a variety of use cases by viewing a live EMA-hosted webcast titled “AIOps Deployments and the Real World: Bringing Operations and Security Together,” which will be held on Tuesday, November 10th at 1:00 pm EST. You can register for the webcast at https://info.enterprisemanagement.com/aiops-deployments-in-the-real-world-webinar-centerity.

About Centerity

Centerity’s Cyber-AIOps Platform with advanced Integrated Security delivers Dynamic Business Service Views of the full technology stack to the executives responsible for technology-driven business services, ensuring the performance, availability and security of critical processes. Centerity displays real-time, consolidated business analytics for complex on-prem, cloud, and hybrid technology environments generating SLA Executive Dashboards that identify performance anomalies and isolate faults across applications, operating systems, infrastructure and cloud assets. Learn more at centerity.com.

To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.

Contact information

Stephen McCarney
Merlin Ventures | Merlin Cyber
smccarney@merlin.vc
703-752-8356

About Business Wire

Business Wire
Business Wire



Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

Celltrion Healthcare presents the first real-world data for Truxima ® (biosimilar rituximab) in patients with diffuse large B-cell lymphoma at the EHA 2021 Virtual Congress12.6.2021 17:45:00 CEST | Press release

Celltrion Healthcare today presented new data from its post-approval study evaluating the real-world clinical effectiveness and safety of Truxima® (biosimilar rituximab, CT-P10) in patients with diffuse large B-cell lymphoma (DLBCL) at the European Hematology Association (EHA) 2021 Virtual Congress.1 CT-P10 was granted European Medicines Agency approval in 2017 for the treatment of rheumatoid arthritis (RA) and specific blood cancers, including non-Hodgkin’s lymphoma (NHL).2 DLBCL is the most common subtype of NHL, representing an estimated 30-40% of adult cases.3,4,5,6 This non-interventional post-authorisation safety study (PASS) involved the collection of patient-level data from hospital medical records for patients with DLBCL who received CT-P10 treatment in five European countries (United Kingdom, Spain, France, Germany and Italy). CT-P10 treatment pattern data were collected retrospectively during the 30-month observation period and patients were selected based on the treatment t

Janssen Announces Results from Phase 3 MAIA Study Showing Significant Overall Survival Benefits for Treatment with DARZALEX ® ▼ (daratumumab) in Patients with Newly Diagnosed Multiple Myeloma Who are Transplant Ineligible12.6.2021 09:01:00 CEST | Press release

The Janssen Pharmaceutical Companies of Johnson & Johnson announced overall survival (OS) results from the Phase 3 MAIA (NCT02252172) study showing the addition of DARZALEX® ▼(daratumumab) to lenalidomide and dexamethasone (D-Rd) resulted in a statistically significant survival benefit over lenalidomide and dexamethasone (Rd) alone in patients with newly diagnosed multiple myeloma (NDMM) who were ineligible for autologous stem cell transplant (ASCT) and were treated to progression.1 These data were featured in the European Hematology Association (EHA) 2021 Virtual Press Briefing and will be presented as a late-breaking abstract during the EHA Virtual Congress (Abstract #LB1901). The prespecified interim analysis for OS found that after a median follow-up of nearly five years (56.2 months), a 32 percent reduction in the risk of death was observed in the D-Rd treatment arm vs. Rd arm.1 Median OS was not reached in either arm [hazard ratio (HR): 0.68, 95 percent confidence interval (CI),

New Phase 3 Study Results Show IMBRUVICA ® (ibrutinib)-Based Combination Regimen as an All-Oral Fixed-Duration Treatment Demonstrated Superior Progression-Free Survival in Adult Patients with Previously Untreated Chronic Lymphocytic Leukaemia12.6.2021 09:00:00 CEST | Press release

The Janssen Pharmaceutical Companies of Johnson & Johnson today announced primary results from the pivotal Phase 3 GLOW study (NCT03462719) evaluating fixed-duration IMBRUVICA® (ibrutinib) plus venetoclax (I+V) compared to chlorambucil plus obinutuzumab (Clb+O) for first-line treatment of elderly or unfit patients with chronic lymphocytic leukaemia (CLL). The study demonstrated superior progression-free survival (PFS) of a once-daily, all-oral, fixed-duration regimen of I+V versus Clb+O as first-line treatment of CLL; the study also showed improved duration of remission and significantly improved depth of remission.1 With I+V, undetectable minimal residual disease (uMRD) in peripheral blood (PB) was sustained by 85 percent of patients one year after end of treatment.1 The safety and tolerability profile of I+V was consistent with CLL treatment in an older population with comorbidities.1 These data were featured in the European Hematology Association (EHA) 2021 Virtual Press Briefing an

Alluzience ® , the first ready-to-use BoNT-A neuromodulator, receives positive decision for use in Europe11.6.2021 11:53:00 CEST | Press release

Galderma today announced that Alluzience® has completed its European decentralized procedure resulting in a positive decision for the first ready-to-use neuromodulator, a wrinkle relaxing injection, in Europe. National approvals will now take place across the region in line with local processes in each country. Designed for precision, Alluzience® is a liquid form of botulinum toxin type A intended for use in adult patients as a treatment to temporarily improve the appearance of moderate to severe glabellar lines (vertical lines between the eyebrows), when the severity of these lines has an important psychological impact on the patient.1 "The introduction of Alluzience® marks a new era in treatment innovation for upper facial lines in Europe. Like many aspects of physical appearance, glabellar lines can have a significant impact on patients’ confidence and wellbeing. I’ve heard first-hand that the transition to living and working in a virtual world has only exacerbated these issues. As

Secure Communities Forum: Behavioural Insights Can Assist Governments in the Post-Pandemic World11.6.2021 10:15:00 CEST | Press release

The Secure Communities Forum, a global collaboration of security professionals, has convened a leading panel of experts to discuss how behavioural science can impact positive social cohesion, build on the concept of positive citizenship, and encourage positive individual behaviours. The virtual event was attended by 134 people from 18 countries. The Secure Communities Forum convened the webinar in response to the ongoing Covid-19 pandemic. Governments and law enforcement agencies have used behavioural science to encourage adherence to public health measures like social distancing and mask-wearing. Lindsay Juarez, Director at Irrational Labs, USA, opened the session, offering the view that we assume humans are rational, which is not the case. She said: “Behavioural science is about setting people up for success and breaking through the noise. Information isn't enough to change behaviour, the decision-making context matters. “People don’t always act in their own long-term best interests,

Luxembourg’s Supercomputer MeluXina is Operational11.6.2021 09:18:00 CEST | Press release

Luxembourg’s high performance computer MeluXina was officially launched on June 7 putting the country on the global map of computer super powers. MeluXina is capable of executing more than 10 Petaflops, the equivalent of 10 million billion calculations per second, which will rank it among the world’s top 50 supercomputers. The petascale computer is powered by green energy and is part-funded under the European High Performance Computing Joint Undertaking. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210611005115/en/ Minister of State Xavier Bettel; His Royal Highness Henri, Grand Duke of Luxembourg; Minister of the Economy Franz Fayot; EuroHPC Joint Undertaking Executive Director Anders Jensen (Photo: Business Wire) In a series of 8 high-performance computers in the EU, MeluXina joins Vega, another petascale supercomputer located in Slovenia, as the first EuroHPC machines to go live. Its innovative modular architecture allo

Vertex and CRISPR Therapeutics Present New Data in 22 Patients With Greater Than 3 Months Follow-Up Post-Treatment With Investigational CRISPR/Cas9 Gene-Editing Therapy, CTX001™ at European Hematology Association Annual Meeting11.6.2021 09:05:00 CEST | Press release

Vertex Pharmaceuticals Incorporated (Nasdaq:VRTX) and CRISPR Therapeutics (Nasdaq:CRSP) today announced new data on 22 patients,with follow-up of at least 3 months, and ranging from 4 months to 26 months, treated with the investigational CRISPR/Cas9-based gene-editing therapy, CTX001, that show a consistent and sustained response to treatment. CTX001 is being investigated in two ongoing Phase 1/2 clinical trials as a potential one-time therapy for patients suffering from transfusion-dependent beta thalassemia (TDT) and severe sickle cell disease (SCD). In total, more than 40 patients have been dosed across both studies to date. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210611005069/en/ All 15 patients with TDT, including six who have the beta zero/beta zero or other severe genotypes, were transfusion-free at last follow-up, and all seven patients with severe SCD were free of vaso-occlusive crises (VOCs) from CTX001 infu

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom