Novardis Consulting

Novardis Consulting company information, Employees & Contact Information

Компания NOVARDIS имеет более 20 лет опыта реализации цифровых проектов для повышения конкурентоспособности бизнеса. Наша команда внедряет enterprise-решения и разрабатывает микросервисы для компаний розничной торговли, дистрибуции, производства ТНП и транспортной логистики. Компания реализует проекты цифровизации и автоматизации бизнес-процессов, а также занимается разработкой ИТ-решений под задачи клиента и последующей их поддержкой. Залог успеха компании – сплоченная команда с 20-летним успешным опытом, состоящая из более чем +400 экспертов в области оптимизации и цифровизации бизнес-процессов, разработки приложений и системной интеграции. Среди клиентов NOVARDIS такие лидеры рынка, как ЛЕНТА, М.Видео-Эльдорадо, Пулково, Heineken, Faberlic, Комус, Рив Гош, МТС, Связной, НЛМК, Северсталь, Детский мир, и другие. География проектов компании: Россия, Германия, Италия, Чехия, Хорватия, Словакия, ЮАР, Мексика, Казахстан. Команда NOVARDIS – надежный партнер по созданию передовых IТ-решений для повышения прибыльности и конкурентоспособности вашего бизнеса. Приглашаем вас стать частью нашей команды. Пришлите резюме (job@novardis.com).

Company Details

Employees
203
Founded
-
Address
Ул. Детская, Д.5а, Санкт-Петербург,199106,russian Federation
Phone
7-812-655-60-01
Email
in****@****dis.com
Industry
It Services And It Consulting
NAICS
Computer Systems Design and Related Services
Other Computer Related Services
Keywords
IT Consulting.
HQ
Санкт-Петербург
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News

Novartis agrees to acquire Avidity Biosciences, an innovator in RNA therapeutics, strengthening its late-stage neuroscience pipeline - Novartis

Novartis agrees to acquire Avidity Biosciences, an innovator in RNA therapeutics, strengthening its late-stage neuroscience pipeline Novartis

Novartis to present new data at AAN, including seven-year disability outcomes and safety analysis of Kesimpta® in people with relapsing multiple sclerosis - Novartis

Novartis to present new data at AAN, including seven-year disability outcomes and safety analysis of Kesimpta® in people with relapsing multiple sclerosis Novartis

The 2025 Eurovision Song Contest - Novartis

The 2025 Eurovision Song Contest Novartis

Our commitment to ethical and responsible use of Artificial Intelligence (AI) - Novartis

Our commitment to ethical and responsible use of Artificial Intelligence (AI) Novartis

Immunology disease research at Novartis - Novartis

Immunology disease research at Novartis Novartis

Managed access programs - Novartis

Managed access programs Novartis

Human rights - Novartis

Human rights Novartis

Compassionate use: Providing access to much needed treatments - Novartis

Compassionate use: Providing access to much needed treatments Novartis

Therapeutic areas - Novartis

Therapeutic areas Novartis

Coronavirus - Novartis

Coronavirus Novartis

Novartis enters agreement to acquire Mariana Oncology, strengthening radioligand therapy pipeline - Novartis

Novartis enters agreement to acquire Mariana Oncology, strengthening radioligand therapy pipeline Novartis

From black holes to AI driven drug discovery – collaboration wins the day - Novartis

From black holes to AI driven drug discovery – collaboration wins the day Novartis

Sub-Saharan Africa - Novartis

Sub-Saharan Africa Novartis

Novartis delivers strong sales growth, robust margin expansion and major innovation milestones. Raises FY guidance - Novartis

Novartis delivers strong sales growth, robust margin expansion and major innovation milestones. Raises FY guidance Novartis

Climate - Novartis

Climate Novartis

Novartis receives FDA approval for Fabhalta® (iptacopan), offering superior hemoglobin improvement in the absence of transfusions as the first oral monotherapy for adults with PNH - Novartis

Novartis receives FDA approval for Fabhalta® (iptacopan), offering superior hemoglobin improvement in the absence of transfusions as the first oral monotherapy for adults with PNH Novartis

FDA approves Novartis Kisqali® to reduce risk of recurrence in people with HR+/HER2- early breast cancer - Novartis

FDA approves Novartis Kisqali® to reduce risk of recurrence in people with HR+/HER2- early breast cancer Novartis

Board of Directors - Novartis

Board of Directors Novartis

Novartis Scemblix® Phase III data first to show superior efficacy with a favorable safety and tolerability profile vs. standard-of-care TKIs in adults with newly diagnosed CML - Novartis

Novartis Scemblix® Phase III data first to show superior efficacy with a favorable safety and tolerability profile vs. standard-of-care TKIs in adults with newly diagnosed CML Novartis

Novartis data show potential of remibrutinib as an oral treatment for chronic spontaneous urticaria providing significant symptom improvement as early as Week 2 - Novartis

Novartis data show potential of remibrutinib as an oral treatment for chronic spontaneous urticaria providing significant symptom improvement as early as Week 2 Novartis

Novartis presents new data on safety and efficacy of Zolgensma, including maintained and improved motor milestones in older and heavier children with SMA - Novartis

Novartis presents new data on safety and efficacy of Zolgensma, including maintained and improved motor milestones in older and heavier children with SMA Novartis

About - Novartis

About Novartis

Novartis bolsters innovative medicines strategy and renal pipeline with agreement to acquire Chinook Therapeutics for USD 3.2bn upfront (USD 40 / share) - Novartis

Novartis bolsters innovative medicines strategy and renal pipeline with agreement to acquire Chinook Therapeutics for USD 3.2bn upfront (USD 40 / share) Novartis

Novartis renews commitment to malaria elimination, investing USD 100 million to research and develop next-generation antimalarials - Novartis

Novartis renews commitment to malaria elimination, investing USD 100 million to research and develop next-generation antimalarials Novartis

Novartis radioligand therapy Lutathera® FDA approved as first medicine specifically for pediatric patients with gastroenteropancreatic neuroendocrine tumors - Novartis

Novartis radioligand therapy Lutathera® FDA approved as first medicine specifically for pediatric patients with gastroenteropancreatic neuroendocrine tumors Novartis

Machine learning poised to accelerate drug discovery - Novartis

Machine learning poised to accelerate drug discovery Novartis

Novartis data show rapid and effective disease activity control with remibrutinib (LOU064) in patients with chronic spontaneous urticaria - Novartis

Novartis data show rapid and effective disease activity control with remibrutinib (LOU064) in patients with chronic spontaneous urticaria Novartis

The data42 program shows Novartis’ intent to go big on data and digital - Novartis

The data42 program shows Novartis’ intent to go big on data and digital Novartis

Novartis investigational iptacopan Phase III study demonstrates clinically meaningful and statistically significant proteinuria reduction in patients with C3 glomerulopathy (C3G) - Novartis

Novartis investigational iptacopan Phase III study demonstrates clinically meaningful and statistically significant proteinuria reduction in patients with C3 glomerulopathy (C3G) Novartis

Novartis acquires Arctos Medical, expanding optogenetics portfolio to bring gene therapies to patients with severe vision loss - Novartis

Novartis acquires Arctos Medical, expanding optogenetics portfolio to bring gene therapies to patients with severe vision loss Novartis

Novartis and Medicines for Malaria Venture announce decision to move to Phase 3 study for novel ganaplacide/lumefantrine-SDF combination in adults and children with malaria - Novartis

Novartis and Medicines for Malaria Venture announce decision to move to Phase 3 study for novel ganaplacide/lumefantrine-SDF combination in adults and children with malaria Novartis

Novartis announces lift of partial clinical trial hold and plans to initiate a new, pivotal Phase 3 study of intrathecal OAV-101 in older patients with SMA - Novartis

Novartis announces lift of partial clinical trial hold and plans to initiate a new, pivotal Phase 3 study of intrathecal OAV-101 in older patients with SMA Novartis

Novartis announces collaboration with Molecular Partners to develop two DARPin® therapies designed for potential use against COVID-19 - Novartis

Novartis announces collaboration with Molecular Partners to develop two DARPin® therapies designed for potential use against COVID-19 Novartis

Novartis Cosentyx® positive 16-week PREVENT results advance potential new indication for patients with axial spondyloarthritis - Novartis

Novartis Cosentyx® positive 16-week PREVENT results advance potential new indication for patients with axial spondyloarthritis Novartis

Novartis Tafinlar® (dabrafenib) + Mekinist® (trametinib) demonstrates unprecedented efficacy in pediatric patients with BRAF V600 low-grade gliomas in Phase II/III study - Novartis

Novartis Tafinlar® (dabrafenib) + Mekinist® (trametinib) demonstrates unprecedented efficacy in pediatric patients with BRAF V600 low-grade gliomas in Phase II/III study Novartis

AveXis Announces Innovative Zolgensma® Gene Therapy Access Programs for US Payers and Families - Novartis

AveXis Announces Innovative Zolgensma® Gene Therapy Access Programs for US Payers and Families Novartis

Novartis expands Zolgensma manufacturing capacity with approval of multi-product North Carolina facility - Novartis

Novartis expands Zolgensma manufacturing capacity with approval of multi-product North Carolina facility Novartis

Novartis receives European Commission approval for Pluvicto® as the first targeted radioligand therapy for treatment of progressive PSMA–positive metastatic castration-resistant prostate cancer - Novartis

Novartis receives European Commission approval for Pluvicto® as the first targeted radioligand therapy for treatment of progressive PSMA–positive metastatic castration-resistant prostate cancer Novartis

Novartis provides update on Phase III study evaluating canakinumab (ACZ885) as second or third-line treatment in combination with chemotherapy in non-small cell lung cancer - Novartis

Novartis provides update on Phase III study evaluating canakinumab (ACZ885) as second or third-line treatment in combination with chemotherapy in non-small cell lung cancer Novartis

Novartis to sell its Roche stake in a bilateral transaction to Roche - Novartis

Novartis to sell its Roche stake in a bilateral transaction to Roche Novartis

Novartis announces positive result of phase III study with radioligand therapy 177Lu-PSMA-617 in patients with advanced prostate cancer - Novartis

Novartis announces positive result of phase III study with radioligand therapy 177Lu-PSMA-617 in patients with advanced prostate cancer Novartis

Novartis receives EU approval for Leqvio®* (inclisiran), a first-in-class siRNA to lower cholesterol with two doses a year - Novartis

Novartis receives EU approval for Leqvio®* (inclisiran), a first-in-class siRNA to lower cholesterol with two doses a year Novartis

European Medicines Agency (EMA) approves safety label update for Novartis Beovu® - Novartis

European Medicines Agency (EMA) approves safety label update for Novartis Beovu® Novartis

Novartis provides update on RUXCOVID study of ruxolitinib for hospitalized patients with COVID-19 - Novartis

Novartis provides update on RUXCOVID study of ruxolitinib for hospitalized patients with COVID-19 Novartis

Novartis expands Oncology pipeline with in-licensing of tislelizumab from BeiGene - Novartis

Novartis expands Oncology pipeline with in-licensing of tislelizumab from BeiGene Novartis

Novartis announces collaboration on HARMONIA, a Phase III, head-to-head trial evaluating Kisqali® vs. Ibrance®* in patients with HR+/HER2- advanced breast cancer - Novartis

Novartis announces collaboration on HARMONIA, a Phase III, head-to-head trial evaluating Kisqali® vs. Ibrance®* in patients with HR+/HER2- advanced breast cancer Novartis

Novartis receives FDA approval for Mayzent® (siponimod), the first oral drug to treat secondary progressive MS with active disease - Novartis

Novartis receives FDA approval for Mayzent® (siponimod), the first oral drug to treat secondary progressive MS with active disease Novartis

World-first agreement between Novartis and the NHS enables broad and rapid access to first-in-class cholesterol-lowering medicine Leqvio® ▼(inclisiran) - Novartis

World-first agreement between Novartis and the NHS enables broad and rapid access to first-in-class cholesterol-lowering medicine Leqvio® ▼(inclisiran) Novartis

Novartis provides an update on Phase III ligelizumab (QGE031) studies in chronic spontaneous urticaria (CSU) - Novartis

Novartis provides an update on Phase III ligelizumab (QGE031) studies in chronic spontaneous urticaria (CSU) Novartis

Novartis receives first ever FDA approval for a CAR-T cell therapy, Kymriah(TM) (CTL019), for children and young adults with B-cell ALL that is refractory or has relapsed at least twice - Novartis

Novartis receives first ever FDA approval for a CAR-T cell therapy, Kymriah(TM) (CTL019), for children and young adults with B-cell ALL that is refractory or has relapsed at least twice Novartis

Novartis enters agreement to acquire AveXis Inc. for USD 8.7 bn to transform care in SMA and expand position as a gene therapy and Neuroscience leader - Novartis

Novartis enters agreement to acquire AveXis Inc. for USD 8.7 bn to transform care in SMA and expand position as a gene therapy and Neuroscience leader Novartis

Novartis reinforces commitment to patient access, pricing a EUR 1.85 billion sustainability-linked bond - Novartis

Novartis reinforces commitment to patient access, pricing a EUR 1.85 billion sustainability-linked bond Novartis

Novartis and Microsoft announce collaboration to transform medicine with artificial intelligence - Novartis

Novartis and Microsoft announce collaboration to transform medicine with artificial intelligence Novartis

Novartis expands Africa Sickle Cell Disease program to Uganda and Tanzania - Novartis

Novartis expands Africa Sickle Cell Disease program to Uganda and Tanzania Novartis

Novartis and Pear Therapeutics to develop digital therapeutics for patients with schizophrenia and multiple sclerosis - Novartis

Novartis and Pear Therapeutics to develop digital therapeutics for patients with schizophrenia and multiple sclerosis Novartis

Novartis announces plan to initiate clinical study of Jakavi® in severe COVID-19 patients and establish international compassionate use program - Novartis

Novartis announces plan to initiate clinical study of Jakavi® in severe COVID-19 patients and establish international compassionate use program Novartis

Novartis and DNDi to collaborate on the development of a new oral drug to treat visceral leishmaniasis - Novartis

Novartis and DNDi to collaborate on the development of a new oral drug to treat visceral leishmaniasis Novartis

Novartis, Amgen and Banner Alzheimer's Institute discontinue clinical program with BACE inhibitor CNP520 for Alzheimer's prevention - Novartis

Novartis, Amgen and Banner Alzheimer's Institute discontinue clinical program with BACE inhibitor CNP520 for Alzheimer's prevention Novartis

Novartis announces completion of transactions with GSK - Novartis

Novartis announces completion of transactions with GSK Novartis

Novartis receives approval from Japanese Ministry of Health, Labour and Welfare for Zolgensma® the only gene therapy for patients with spinal muscular atrophy (SMA) - Novartis

Novartis receives approval from Japanese Ministry of Health, Labour and Welfare for Zolgensma® the only gene therapy for patients with spinal muscular atrophy (SMA) Novartis

Novartis five-year Kymriah® data show durable remission and long-term survival maintained in children and young adults with advanced B-cell ALL - Novartis

Novartis five-year Kymriah® data show durable remission and long-term survival maintained in children and young adults with advanced B-cell ALL Novartis

Novartis expands Kymriah® manufacturing footprint with first-ever approved site for commercial CAR-T cell therapy manufacturing in Asia - Novartis

Novartis expands Kymriah® manufacturing footprint with first-ever approved site for commercial CAR-T cell therapy manufacturing in Asia Novartis

Novartis Cosentyx® gains fourth indication in EU with first-in-class approval in axial spondyloarthritis spectrum - Novartis

Novartis Cosentyx® gains fourth indication in EU with first-in-class approval in axial spondyloarthritis spectrum Novartis

Novartis received European Medicines Agency (EMA) PRIME designation for iptacopan (LNP) in C3 glomerulopathy (C3G) - Novartis

Novartis received European Medicines Agency (EMA) PRIME designation for iptacopan (LNP) in C3 glomerulopathy (C3G) Novartis

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