[Rapporto di ricerca] Il mercato dei software di farmacovigilanza e sicurezza dei farmaci dovrebbe raggiungere 292,97 milioni di dollari nel 2027 da 160,67 milioni di dollari nel 2019. Si stima che il mercato crescerà con un CAGR del 7,6% dal 2020-2027 .
L'ambito del mercato del software di farmacovigilanza e sicurezza dei farmaci comprende il tipo di software, il tipo di prodotto, l'utente finale e la regione. Il mercato dei software di farmacovigilanza e sicurezza dei farmaci, in base alla regione, è segmentato in Nord America, Europa, Asia Pacifico, Medio Oriente e Stati Uniti. Africa e America meridionale e centrale. Il rapporto offre approfondimenti e analisi approfondite del mercato del software di farmacovigilanza e sicurezza dei farmaci, sottolineando vari parametri quali tendenze del mercato, progressi tecnologici, dinamiche di mercato e analisi del panorama competitivo dei principali attori del mercato in tutto il mondo. mondo. Include anche l'analisi dell'impatto del COVID-19 in tutte le regioni.
Regioni redditizie per il mercato dei software di farmacovigilanza e sicurezza dei farmaci
Approfondimenti di mercato
< p>Globalizzazione della farmacovigilanzaLa farmacovigilanza è il processo di monitoraggio e valutazione delle reazioni avverse ai farmaci ed è una componente chiave di efficaci sistemi di regolamentazione dei farmaci, pratica clinica e programmi di sanità pubblica. Il numero di reazioni avverse ai farmaci (ADR) segnalate ha comportato un aumento del volume di dati gestiti. Nell'attuale rete globale di centri di farmacovigilanza coordinati dall'Osservatorio di Uppsala. La farmacovigilanza è una parte fondamentale e integrante della ricerca clinica e oggigiorno sta crescendo in molti paesi. Oggi molti centri di farmacovigilanza stanno lavorando per il monitoraggio della sicurezza dei farmaci in questo ambito globale, tuttavia, all'inizio del millennio la farmacovigilanza si trova ad affrontare sfide importanti in termini di migliore sicurezza e monitoraggio dei farmaci.
La segnalazione e l'archiviazione centralizzata dei dati le segnalazioni di reazioni avverse ai farmaci aiuteranno a monitorare e prevenire future reazioni avverse al farmaco. Rafforzamento dell'Agenzia europea per i medicinali (EMA) e della Food and Drug Administration (FDA) statunitense nell'area della farmacovigilanza attraverso l'interazione su diversi argomenti relativi alla sicurezza post-marketing e allo scambio scientifico. Discussioni su priorità come biosimilari, medicinali per il trattamento del cancro, medicinali orfani, medicinali per bambini e prodotti a base di sangue, tra gli altri argomenti.
Pertanto, l'aumento della globalizzazione nel settore della farmacovigilanza aiuta i software per la sicurezza dei farmaci. Migliora la qualità e l'efficacia del software di farmacovigilanza e di sicurezza dei farmaci e si prevede che favorirà la crescita del mercato durante il periodo di previsione.
Approfondimenti basati sul tipo di software
Basato sul tipo di software il mercato è segmentato in software di segnalazione degli eventi avversi, software di audit sulla sicurezza dei farmaci, software di monitoraggio dei problemi e software completamente integrato. Nel 2019, il segmento dei software per la segnalazione di eventi avversi deteneva la quota maggiore del mercato, per software. Tuttavia, si prevede che il segmento del software completamente integrato crescerà al ritmo più elevato durante il periodo di previsione grazie alla sua accuratezza nell'evitare la ridondanza dei dati eliminando gli errori e monitorando i rapporti sulla sicurezza dei singoli casi.
Mercato globale dei software per la farmacovigilanza e la sicurezza dei farmaci, per tipo di software: 2019 e 2027Approfondimenti basati sulla modalità di consegna
In base alla modalità di consegna, il mercato viene segmentato in on-premise e basato su cloud. Nel 2019, il segmento on-premise deteneva la quota maggiore del mercato, per modalità di consegna. Tuttavia, si prevede che il segmento basato sul cloud crescerà al ritmo più rapido nei prossimi anni grazie ai vantaggi associati come l'accesso remoto ai dati e il monitoraggio dei dati in tempo reale.
Approfondimenti basati sull'utente finale
In base all'utente finale, il mercato è segmentato in aziende farmaceutiche e biotecnologiche, organizzazioni di ricerca a contratto (CRO) e aziende di outsourcing dei processi aziendali (BPO). Nel 2019, il segmento delle organizzazioni di ricerca a contratto deteneva la quota maggiore del mercato, per utente finale. Inoltre, si prevede che il segmento delle organizzazioni di ricerca a contratto crescerà al ritmo più rapido nei prossimi anni a causa dell'aumento delle attività di scoperta di farmaci nelle aziende farmaceutiche.
Approfondimenti strategici
Strategie inorganiche come partnership, fusioni e acquisizioni sono comunemente adottate dalle aziende per soddisfare le mutevoli richieste dei clienti e mantenere il proprio marchio in tutto il mondo. Gli operatori di mercato che operano nel mercato dei software di farmacovigilanza e sicurezza dei farmaci adottano anche strategie organiche come il lancio e l'espansione dei prodotti per ampliare la propria presenza e il portafoglio di prodotti in tutto il mondo e per soddisfare la crescente domanda.
Per tipo di software
- Software completamente integrato
- Software di segnalazione di eventi avversi
- Software per controlli sulla sicurezza dei farmaci
- Software per il monitoraggio dei problemi
Per modalità di consegna
- Basato sul cloud< /li>
- In sede
Per utente finale
- Organizzazioni di ricerca a contratto
- Aziende farmaceutiche e biotecnologiche
- Outsourcing dei processi aziendali
Per area geografica
- Nord America
- Stati Uniti< /li>
- Canada
- Messico
- Europa
- Francia
- Germania
- Italia
- Regno Unito
- Spagna
- Resto d'Europa
- Asia Pacifico (APAC)
- Cina
- India
- Corea del Sud
- Giappone
- Australia
- Resto dell'APAC
- Medio Oriente e Stati Uniti Africa (MEA)
- Sudafrica
- Arabia Saudita
- EAU
- Resto del MEA
- America centrale e meridionale (SCAM)
- Brasile
- Argentina
- Resto dello SCAM
- Veeva Systems   ; '   ;
- IQVIA Inc. &n bsp;
- Ennov ; '   ; '
- AB Cubo &n bsp;
- United Biosource LLC ;
- ArisGlobal LLC
- Sparta Systems
- Oracle Corporation
- Sarjen Systems Pvt. Ltd. nbsp;
- EXTEDO ; '   ;
- Applicazione massima ; '
- Applicazioni aziendali online, Inc.
Profili aziendali
Report Coverage
Revenue forecast, Company Analysis, Industry landscape, Growth factors, and Trends
Segment Covered
This text is related
to segments covered.
Regional Scope
North America, Europe, Asia Pacific, Middle East & Africa, South & Central America
Country Scope
This text is related
to country scope.
Frequently Asked Questions
Pharmacovigilance (PV) plays an important role in drug monitoring and identification of drug interactions with human. The fully integrated software segment are expected to contribute in the growth of pharmacovigilance and drug safety market.
Rising incidences of adverse drug reaction (ADR) and globalization of pharmacovigilance have been boosting the market over the years. However, the expensive technology are likely to have a negative impact on the growth of the market in the coming years.
The costs of the pharmacovigilance and drug safety software are much higher, and they may cost US$ 1,0000–5,0000, or more, per software. The cost may also differ from product to product and software types.
The List of Companies - Pharmacovigilance and Drug Safety Software Market
- Veeva Systems
- IQVIA Inc.
- Ennov
- AB Cube
- United Biosource LLC
- ArisGlobal LLC
- Sparta Systems
- Oracle Corporation
- Sarjen Systems Pvt. Ltd
- EXTEDO
- Maxapplication
- Online Business Applications, Inc.
The Insight Partners performs research in 4 major stages: Data Collection & Secondary Research, Primary Research, Data Analysis and Data Triangulation & Final Review.
- Data Collection and Secondary Research:
As a market research and consulting firm operating from a decade, we have published and advised several client across the globe. First step for any study will start with an assessment of currently available data and insights from existing reports. Further, historical and current market information is collected from Investor Presentations, Annual Reports, SEC Filings, etc., and other information related to company’s performance and market positioning are gathered from Paid Databases (Factiva, Hoovers, and Reuters) and various other publications available in public domain.
Several associations trade associates, technical forums, institutes, societies and organization are accessed to gain technical as well as market related insights through their publications such as research papers, blogs and press releases related to the studies are referred to get cues about the market. Further, white papers, journals, magazines, and other news articles published in last 3 years are scrutinized and analyzed to understand the current market trends.
- Primary Research:
The primarily interview analysis comprise of data obtained from industry participants interview and answers to survey questions gathered by in-house primary team.
For primary research, interviews are conducted with industry experts/CEOs/Marketing Managers/VPs/Subject Matter Experts from both demand and supply side to get a 360-degree view of the market. The primary team conducts several interviews based on the complexity of the markets to understand the various market trends and dynamics which makes research more credible and precise.
A typical research interview fulfils the following functions:
- Provides first-hand information on the market size, market trends, growth trends, competitive landscape, and outlook
- Validates and strengthens in-house secondary research findings
- Develops the analysis team’s expertise and market understanding
Primary research involves email interactions and telephone interviews for each market, category, segment, and sub-segment across geographies. The participants who typically take part in such a process include, but are not limited to:
- Industry participants: VPs, business development managers, market intelligence managers and national sales managers
- Outside experts: Valuation experts, research analysts and key opinion leaders specializing in the electronics and semiconductor industry.
Below is the breakup of our primary respondents by company, designation, and region:
Once we receive the confirmation from primary research sources or primary respondents, we finalize the base year market estimation and forecast the data as per the macroeconomic and microeconomic factors assessed during data collection.
- Data Analysis:
Once data is validated through both secondary as well as primary respondents, we finalize the market estimations by hypothesis formulation and factor analysis at regional and country level.
- Macro-Economic Factor Analysis:
We analyse macroeconomic indicators such the gross domestic product (GDP), increase in the demand for goods and services across industries, technological advancement, regional economic growth, governmental policies, the influence of COVID-19, PEST analysis, and other aspects. This analysis aids in setting benchmarks for various nations/regions and approximating market splits. Additionally, the general trend of the aforementioned components aid in determining the market's development possibilities.
- Country Level Data:
Various factors that are especially aligned to the country are taken into account to determine the market size for a certain area and country, including the presence of vendors, such as headquarters and offices, the country's GDP, demand patterns, and industry growth. To comprehend the market dynamics for the nation, a number of growth variables, inhibitors, application areas, and current market trends are researched. The aforementioned elements aid in determining the country's overall market's growth potential.
- Company Profile:
The “Table of Contents” is formulated by listing and analyzing more than 25 - 30 companies operating in the market ecosystem across geographies. However, we profile only 10 companies as a standard practice in our syndicate reports. These 10 companies comprise leading, emerging, and regional players. Nonetheless, our analysis is not restricted to the 10 listed companies, we also analyze other companies present in the market to develop a holistic view and understand the prevailing trends. The “Company Profiles” section in the report covers key facts, business description, products & services, financial information, SWOT analysis, and key developments. The financial information presented is extracted from the annual reports and official documents of the publicly listed companies. Upon collecting the information for the sections of respective companies, we verify them via various primary sources and then compile the data in respective company profiles. The company level information helps us in deriving the base number as well as in forecasting the market size.
- Developing Base Number:
Aggregation of sales statistics (2020-2022) and macro-economic factor, and other secondary and primary research insights are utilized to arrive at base number and related market shares for 2022. The data gaps are identified in this step and relevant market data is analyzed, collected from paid primary interviews or databases. On finalizing the base year market size, forecasts are developed on the basis of macro-economic, industry and market growth factors and company level analysis.
- Data Triangulation and Final Review:
The market findings and base year market size calculations are validated from supply as well as demand side. Demand side validations are based on macro-economic factor analysis and benchmarks for respective regions and countries. In case of supply side validations, revenues of major companies are estimated (in case not available) based on industry benchmark, approximate number of employees, product portfolio, and primary interviews revenues are gathered. Further revenue from target product/service segment is assessed to avoid overshooting of market statistics. In case of heavy deviations between supply and demand side values, all thes steps are repeated to achieve synchronization.
We follow an iterative model, wherein we share our research findings with Subject Matter Experts (SME’s) and Key Opinion Leaders (KOLs) until consensus view of the market is not formulated – this model negates any drastic deviation in the opinions of experts. Only validated and universally acceptable research findings are quoted in our reports.
We have important check points that we use to validate our research findings – which we call – data triangulation, where we validate the information, we generate from secondary sources with primary interviews and then we re-validate with our internal data bases and Subject matter experts. This comprehensive model enables us to deliver high quality, reliable data in shortest possible time.
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