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Asia Pacific Pharmacovigilance Market Size, Share & Trends Analysis Report By Service Provider (In-house, Contract Outsourcing), By Product Life Cycle, By Therapeutic Area, By Process Flow, By End Use, By Type,- Industry Analysis, Size, Share, Growth, Tr

Publisher Nova One Advisor
Published May 26, 2025
Length 469 Pages
SKU # ONEA20057891

Description

Asia Pacific Pharmacovigilance Market Size and Growth
The Asia Pacific pharmacovigilance market size was exhibited at USD 2.85 billion in 2023 and is projected to hit around USD 6.56 billion by 2033, growing at a CAGR of 8.7% during the forecast period 2024 to 2033.

Asia Pacific Pharmacovigilance Market Key Takeaways:

The phase IV segment led the market and accounted for the largest revenue share of 75.8% in 2023.
The contract outsourcing service providers segment dominated the market and accounted for the largest revenue share of 60.8% in 2023.
The spontaneous reporting segment accounted for the largest revenue share of 30.2% in 2023
The pharmaceutical segment accounted for the largest revenue share of 40.1% in 2023.
The biotechnology companies segment is expected to grow at a CAGR of 9.2% from 2024 to 2033
The oncology segment led the market and accounted for a revenue share of 27.2% in 2023.
The signal detection segment dominated the APAC regional market, accounting for the highest revenue share of 40.0% in 2023.
The case data management segment is anticipated to grow at a CAGR of 8.8% from 2024 to 2033.

Market Overview
The Asia Pacific pharmacovigilance market is rapidly evolving, supported by growing pharmaceutical R&D, expanding clinical trial activity, and the region’s increasing contribution to global drug manufacturing and innovation. Pharmacovigilance—the science and activities related to detecting, evaluating, understanding, and preventing adverse drug reactions (ADRs)—has become a pivotal component in drug development and healthcare delivery across Asia Pacific.
Traditionally dominated by North America and Europe, the global pharmacovigilance landscape is witnessing a significant geographic shift, with countries like India, China, Japan, and South Korea emerging as vital contributors. Governments across the region are now enforcing stronger post-marketing surveillance requirements, while multinational pharmaceutical companies are investing in local safety infrastructure to meet global compliance standards.
The growing volume of clinical trials, particularly in oncology, neurology, and infectious diseases, is amplifying the demand for safety monitoring. With an expanding patient population and increasing access to prescription drugs, pharmacovigilance systems are required not just to ensure regulatory compliance but also to protect public health. This has opened new growth avenues for contract outsourcing firms, AI-based pharmacovigilance platforms, and data-driven safety analytics providers.
Importantly, pharmacovigilance is transitioning from a cost center to a strategic differentiator. Companies leveraging advanced safety analytics, real-world evidence (RWE), and electronic health records (EHRs) for signal detection are better positioned to respond proactively to safety issues, thus enhancing product longevity and brand trust. The Asia Pacific market is poised for robust growth through this decade, underpinned by its rising healthcare digitization and harmonization with international regulatory standards.
Major Trends in the Market

Globalization of Drug Safety Compliance: Increasing alignment of regional regulatory frameworks with ICH and WHO guidelines for pharmacovigilance reporting and monitoring.

Expansion of Clinical Trials: Surge in Phase III and IV trials across India, China, and South Korea driving demand for sophisticated pharmacovigilance services.

AI-Enabled Signal Detection: Adoption of AI and machine learning algorithms for automation of ADR reporting and predictive analytics.

Rise of Local PV Outsourcing Firms: Emergence of domestic CROs and pharmacovigilance service providers offering scalable, cost-effective safety operations.

Real-World Data Integration: Increasing use of hospital data, EHRs, and patient registries for post-marketing surveillance and adverse event tracking.

Digital Adverse Event Reporting Tools: Deployment of mobile apps and web-based portals for direct patient ADR reporting.

COVID-19 and Vaccine Safety Monitoring: Strengthened infrastructure and vigilance systems due to pandemic-driven pharmacovigilance efforts.

Report Scope of Asia Pacific Pharmacovigilance Market

Report Coverage
Details

Market Size in 2024
USD 3.10 Billion

Market Size by 2033
USD 6.56 Billion

Growth Rate From 2024 to 2033
CAGR of 8.7%

Base Year
2023

Forecast Period
2024-2033

Segments Covered
Product life cycle, Service Provider, Type, End use, Therapeutic Area, Process Flow, Country

Market Analysis (Terms Used)
Value (US$ Million/Billion) or (Volume/Units)

Country scope
Japan; China; India; Australia; South Korea; Thailand

Key Companies Profiled
Dr. Reddy’s Laboratories Ltd.; Sun Pharmaceutical Industries Ltd.; Cipla Inc.; Aurobindo Pharma.; Asymchem Laboratories; Reyoung Pharmaceutical; CSPC Pharmaceutical Group Limited; Otsuka Pharmaceutical Australia Pty Ltd.; GC Biopharma Corp.; Chong Kun Dang Pharmaceutical Corporation.

Key Market Driver
Boom in Clinical Trials Across Asia Pacific
One of the most significant drivers in the Asia Pacific pharmacovigilance market is the exponential rise in clinical trial activity across the region. Countries like India, China, and South Korea have become hotbeds for global clinical trials due to their large patient pools, cost-effective research environments, and improving regulatory transparency. As these trials progress through later phases, pharmacovigilance becomes critical to monitor trial-related adverse events, ensure patient safety, and secure regulatory approvals.
For example, India’s New Drugs and Clinical Trials Rules, 2019 mandate rigorous safety reporting mechanisms, while China’s National Medical Products Administration (NMPA) now emphasizes pharmacovigilance compliance for both domestic and foreign manufacturers. These developments significantly increase the need for advanced pharmacovigilance platforms, staff training, and AI-integrated solutions to manage high volumes of safety data efficiently.
Key Market Restraint
Fragmented Regulatory Framework Across Countries
Despite considerable progress, the pharmacovigilance ecosystem in Asia Pacific is still hindered by non-uniform and evolving regulatory landscapes. While countries like Japan and Australia have mature pharmacovigilance systems aligned with ICH guidelines, other markets like Thailand and Indonesia are still developing their frameworks. This lack of standardization increases complexity for pharmaceutical companies conducting multi-country trials or post-marketing surveillance across the region.
Inconsistencies in ADR reporting requirements, data formats, timelines, and language barriers add to the operational burden. Additionally, limited awareness among healthcare professionals and the general public regarding adverse event reporting reduces the volume and quality of data collected. These challenges necessitate customized pharmacovigilance strategies for each market, driving up costs and limiting scalability.
Key Market Opportunity
AI-Driven Pharmacovigilance Platforms for Scalable Growth
As the volume of adverse event data grows, the application of AI and natural language processing (NLP) in pharmacovigilance presents a transformative opportunity for the Asia Pacific market. AI-based platforms can automate case intake, coding, causality assessment, and signal detection reducing manual workload and minimizing errors.
In India and China, startups and global tech companies are piloting platforms that integrate with EHR systems and tap into unstructured data from call centers, social media, and medical literature. These tools offer predictive safety insights, enhance regulatory readiness, and accelerate decision-making. With supportive policies around digital health, increasing cloud infrastructure adoption, and growing acceptance of AI by regulators, AI-enabled pharmacovigilance is set to disrupt traditional workflows and offer significant competitive advantage.
Asia Pacific Pharmacovigilance Market By Product Life Cycle Insights
Phase IV pharmacovigilance held the dominant share in the Asia Pacific market due to the region’s increasing focus on post-marketing drug surveillance and patient safety. Once drugs are approved and released to the market, Phase IV activities ensure the long-term safety and effectiveness of these products in real-world populations. Regulatory bodies in countries like Japan and South Korea have implemented strict pharmacovigilance obligations post-approval, requiring manufacturers to conduct post-marketing studies, submit periodic safety update reports (PSURs), and manage risk mitigation plans. These requirements have led to robust growth in Phase IV pharmacovigilance services, particularly among multinationals launching products in the region.
Meanwhile, Phase III is experiencing the fastest growth, driven by the rising number of late-stage clinical trials across Asia Pacific. Countries like China and India are home to hundreds of Phase III studies annually, requiring constant safety monitoring. Regulatory agencies are increasing their oversight of adverse event data generated during clinical research. This growth is further accelerated by the influx of foreign pharmaceutical sponsors outsourcing safety monitoring to local CROs with Phase III expertise. Technologies like electronic data capture (EDC) and real-time safety signal monitoring are increasingly being deployed to enhance trial efficiency and compliance.
Asia Pacific Pharmacovigilance Market By Service Provider Insights
Contract outsourcing was the leading service provider category due to the rising trend of pharmaceutical companies outsourcing pharmacovigilance functions to local and regional CROs. Outsourcing enables firms to scale operations, reduce costs, and access specialized safety expertise without building internal teams. In Asia Pacific, a growing number of BPO and CRO firms offer end-to-end pharmacovigilance services, from case data management to signal detection and risk mitigation. The maturity of India’s outsourcing industry, the rise of Chinese pharmacovigilance consultancies, and Japan’s hybrid outsourcing models all support this segment’s dominance.
Nonetheless, in-house pharmacovigilance services are expected to grow, particularly among large pharmaceutical and biotech firms in Japan and China who seek tighter control over data privacy, regulatory reporting, and product lifecycle management. These organizations are investing in proprietary safety platforms, EHR integration, and AI-based signal detection to build internal pharmacovigilance capabilities. In-house systems also support real-time cross-functional collaboration, especially for complex or innovative therapies, including biologics and cell-based therapies.
Asia Pacific Pharmacovigilance Market By Type Insights
Spontaneous reporting was the most utilized pharmacovigilance type in Asia Pacific, especially as the foundation for national drug safety surveillance systems. Countries like India (PvPI), China (CADRMP), and Japan (PMDA) have established centralized reporting portals and programs encouraging healthcare professionals and consumers to report suspected adverse reactions. These spontaneous reports are critical for early signal detection, regulatory review, and public health alerts.
However, EHR mining is growing rapidly as healthcare digitization expands across Asia Pacific. Hospitals and health systems are increasingly equipped with electronic medical record systems, especially in urban centers. Real-world data extracted from these records is proving valuable in detecting adverse events that may be underreported in traditional systems. For example, China’s health tech initiatives under the “Healthy China 2030” framework are enabling pilot projects using EHR mining for oncology and cardiovascular drugs. South Korea’s big data initiatives also aim to integrate EHRs into national pharmacovigilance networks.
Asia Pacific Pharmacovigilance Market By End Use Insights
Pharmaceutical companies were the largest end users of pharmacovigilance services, driven by their need to comply with global regulations and maintain post-marketing surveillance. These companies—especially multinationals—run large drug portfolios across multiple Asia Pacific countries, necessitating strong pharmacovigilance infrastructure. In addition to outsourcing safety operations, many pharma firms maintain regional safety hubs in countries like Singapore and India to manage local reporting and regulatory compliance.
Meanwhile, biotechnology companies are projected to grow fastest in the pharmacovigilance space. The biotech sector in Asia Pacific is thriving, with innovative therapies entering clinical trials in immunology, rare diseases, and oncology. As these firms move from early-stage development to late-phase trials and commercialization, they are under pressure to implement robust pharmacovigilance systems. Increasing regulatory focus on biologicals and personalized medicine products is further accelerating this trend.
Asia Pacific Pharmacovigilance Market By Therapeutic Area Insights
Oncology continued to dominate the therapeutic segmentation due to the high incidence of cancer in Asia Pacific and the complexity of oncology drug regimens. Immuno-oncology, targeted therapies, and biosimilars demand rigorous safety monitoring due to their severe and often unpredictable adverse events. Regulatory authorities in Japan and Australia have outlined pharmacovigilance frameworks tailored for cancer drugs, including risk evaluation strategies and mandatory post-marketing safety studies.
Neurology is emerging as a high-growth therapeutic area for pharmacovigilance. With rising prevalence of neurological disorders such as Alzheimer’s, epilepsy, and Parkinson’s disease, more drugs are being developed and tested in this domain. These treatments often require chronic administration and involve unique safety considerations like psychiatric side effects or neurological deterioration. Asia Pacific’s aging population and improved diagnostic capabilities are contributing to this trend, prompting regulators and drug developers to expand safety monitoring efforts in neurology.
Asia Pacific Pharmacovigilance Market By Process Flow Insights
Signal detection, on the other hand, is the fastest-growing process area. With growing volumes of safety data from clinical trials, spontaneous reports, and EHRs, organizations are investing in AI-based systems that can identify emerging safety trends before they become widespread issues. Countries like India and China are encouraging proactive signal detection through public-private collaborations and digital health projects. For example, the Japan PMDA's investment in data mining tools for periodic signal analysis underscores the region’s emphasis on early risk identification.

Case data management dominated process flow activities, reflecting its foundational role in pharmacovigilance operations. Collecting, validating, coding, and submitting individual case safety reports (ICSRs) are regulatory requirements across all major Asia Pacific countries. Most companies deploy standardized tools or third-party platforms to manage high volumes of cases across multiple languages and jurisdictions. The increasing use of automation in this area—such as auto-narrative generation and MedDRA coding—is improving turnaround time and efficiency.
Country Insights
Japan
Japan has one of the most advanced pharmacovigilance infrastructures in Asia. The Pharmaceuticals and Medical Devices Agency (PMDA) mandates detailed risk management plans and supports spontaneous reporting systems. Japanese pharma companies also invest heavily in in-house pharmacovigilance and predictive analytics.
China
China’s NMPA has dramatically reformed its drug safety regulations in recent years. The establishment of the CADRMP and integration with hospital data systems are positioning China as a growing pharmacovigilance hub. Domestic CROs are increasingly partnering with multinationals for local safety monitoring.
India
India’s Pharmacovigilance Programme of India (PvPI) is one of the most active national reporting systems globally. With a large outsourcing industry, India is a preferred destination for pharmacovigilance BPO services. Startups and software companies are also entering the space with AI-enabled solutions.
Australia
Australia's Therapeutic Goods Administration (TGA) follows strict pharmacovigilance standards aligned with ICH guidelines. The country has a strong clinical research infrastructure and uses national registries for post-marketing surveillance.
South Korea
South Korea is a leader in digital health and big data integration. The Korea Institute of Drug Safety and Risk Management (KIDS) oversees ADR monitoring, and the government promotes EHR integration and real-world data analysis for signal detection.
Thailand
Thailand is developing its pharmacovigilance capabilities with assistance from WHO and international agencies. The Thai FDA is working to improve reporting practices and harmonize its systems with ASEAN and ICH standards.
Asia Pacific Pharmacovigilance Market Recent Developments

March 2025 – Novartis partnered with an Indian BPO to establish a pharmacovigilance center for Asia Pacific operations, focusing on automation and EHR integration.

January 2025 – Tata Consultancy Services announced the expansion of its AI-based pharmacovigilance suite in Japan and Australia to enhance signal detection.

November 2024 – China's NMPA launched a real-world data initiative for pharmacovigilance, linking hospital data with national safety reporting systems.

October 2024 – Samsung Biologics in South Korea initiated a collaboration with a local CRO to develop a pharmacovigilance infrastructure for its biosimilar products.

Some of the prominent players in the Asia Pacific pharmacovigilance market include:

Clinquest group B.V. (LINICAL AMERICAS)
Take Solutions Limited
WIPRO
Fosun Pharma
Sinopharm
Sinovac Biotech
Daewoong Pharmaceutical
ALTEOGEN Inc.
A.N.B. Laboratories Co., Ltd.
Biopharm Chemicals Co., Ltd.

Segments Covered in the Report
This report forecasts revenue growth at country levels and provides an analysis of the latest industry trends in each of the sub-segments from 2021 to 2033. For this study, Nova one advisor, Inc. has segmented the Asia Pacific pharmacovigilance market.
Product Life Cycle

Pre-clinical
Phase I
Phase II
Phase III
Phase IV

Service Provider

In-house
Contract Outsourcing

Type

Spontaneous Reporting
Intensified ADR Reporting
Targeted Spontaneous Reporting
Cohort Event Monitoring
EHR Mining

End Use

Pharmaceuticals
Biotechnology Companies
Medical Device Manufacturers
Others

Therapeutic Area

Oncology
Neurology
Cardiology
Respiratory Systems
Other

Process Flow

Case Data Management
Signal Detection
Risk Management System

Country

Japan
China
India
Australia
South Korea
Thailand

Table of Contents

469 Pages
Chapter 1 Research Methodology & Scope
1.1 Market Segmentation & Scope
1.1.1 Product Life Cycle
1.1.2 Service Provider
1.1.3 Type
1.1.4 Process Flow
1.1.5 Therapeutic Area
1.1.6 End Use
1.1.7 Regional Scope
1.1.8 Estimates and Forecast Timeline
1.2 Research Methodology
1.3 Information Procurement
1.3.1 Purchased Database:
1.3.2 Internal Database
1.3.3 Secondary Sources
1.3.4 Primary Research:
1.3.5 Details Of Primary Research
1.3.5.1 Data for primary interviews in North America
1.3.5.2 Data for Primary Interviews in Europe
1.3.5.3 Data for Primary Interviews in Asia Pacific
1.3.5.4 Data for Primary Interviews in Latin America
1.3.5.5 Data for Primary Interviews in Middle East & Africa
1.4 Information or Data Analysis
1.4.1 Data Analysis Models
1.5 Market Formulation & Validation
1.6 Model Details
1.6.1 Commodity Flow Analysis
1.6.1.1 Top down market estimation
1.6.1.2 CAGR Calculation
1.6.1.3 Key Report Updates
1.7 List of Secondary Sources
1.8 List of Abbreviations
1.9 Market Definitions
1.10 Report Objectives
1.10.1 Objective 1:
1.10.2 Objective 2:
Chapter 2 Executive Summary
2.1 Market Snapshot
2.2 Segment Snapshot (Product Life Cycle & Service Provider)
2.3 Segment Snapshot (Type & Therapeutic Area)
2.4 Segment Snapshot (Process Flow & End Use)
2.5 Competitive Landscape Snapshot
Chapter 3 Pharmacovigilance Market Variables, Trends & Scope
3.1 Market Lineage Outlook
3.1.1 Parent Market Analysis
3.1.2 Ancillary Market Analysis
3.2 Penetration & Growth Prospect Mapping
3.3 Pharmacovigilance Market Dynamics
3.3.1 Market Driver Analysis
3.3.1.1 Growing drug consumption and drug development rates
3.3.1.2 Increasing incidence of ADR and drug toxicity
3.3.1.3 Increasing trend of outsourcing pharmacovigilance services
3.3.1.4 Increasing externalization of clinical trial studies by large pharmaceutical and biopharmaceutical companies
3.3.1.5 Increasing regulatory Burden on Manufacturers
3.3.1.6 Introduction of technologically advanced software services
3.3.1.7 Constantly rising investment on R&D by healthcare companies
3.3.1.8 Partnerships and collaborations between market players
3.3.2 Market Restraint Analysis
3.3.2.1 Shortage of skilled labor
3.3.2.2 Expensive technology for small and mid-sized player
3.3.2.3 Lack of recognition
3.3.2.4 Scarcity of integration standards
3.3.3 Industry Challenges
3.4 Pharmacovigilance Market Analysis Tools: Porters
3.5 SWOT Analysis, by Factor (Political & Legal, Economic, and Technological)
3.6 Value Chain Analysis
3.6.1 Preclinical
3.6.2 Clinical
3.6.3 PMA
3.7 Mapping of Life Cycle against Service Offering and Their Demand
3.8 Regulatory Framework
3.8.1 List of Regulatory Bodies by Country
3.9 Organization Structure Introduction
3.10 Pricing Models
3.10.1 Drug Safety Budget Allocation by Activities
3.10.2 By Development Phase
3.10.3 By Therapeutic Area
3.10.4 Pricing Level
3.10.4.1 Project management
3.10.4.2 Case processing
3.10.4.3 ADR Reporting
3.10.4.4 Medical writing
3.10.4.5 Drug safety management
3.11 Technology Timeline Overview
3.11.1 Changing Technology & Adoption
3.11.1.1 Social Media
3.11.1.2 Literature screening
3.11.1.3 Automation and AI
3.11.1.4 Big data analytics in PV
3.12 Impact of COVID-19
3.12.1 Recent Developments & Strategic Outcomes
3.12.1.1 Regulatory requirements/changes due to covid-19
3.12.2 Strategies Implemented by Companies
3.12.2.1 IQVIA
3.12.2.2 PARAXEL International Corporation
3.12.2.3 Bioclinica
3.12.2.4 Pharmaceutical Product Development (PPD)
3.12.2.5 IBM Corporation
3.12.2.6 ICON, plc
3.12.2.7 PRA Health Sciences
3.12.2.8 Covance Inc.
3.12.2.9 ArisGlobal
3.12.2.10 Linical Accelovance
3.12.2.11 Laboratory Corporation of America Holdings
3.13 Market Trends
3.13.1 Scaling Of Resources
3.13.2 Automation in Pharmacovigilance
3.14 Impact of Inflation
3.15 Comparative Analysis between Medical Writing vs Medical Safety Review
3.15.1 Medical Writing Market Outlook, 2022
3.15.1.1 Medical writing Market estimates and forecasts, 2021- 2033
3.15.2 Medical Safety Review Market Outlook, 2022
3.15.2.1 Medical Safety Review market estimates and forecasts, 2021- 2033
Chapter 4 Pharmacovigilance Market: Product Life Cycle Estimates & Trend Analysis
4.1 Product Life Cycle Market Share Analysis, 2022 & 2030
4.2 Product Life Cycle Dashboard
4.3 Market definition and scope
4.3.1 Preclinical
4.3.1.1 Preclinical market estimates and forecasts, 2021- 2033
4.3.2 Phase I
4.3.2.1 Phase I market estimates and forecasts, 2021- 2033
4.3.3 Phase II
4.3.3.1 Phase II market estimates and forecasts, 2021- 2033
4.3.4 Phase III
4.3.4.1 Phase III market estimates and forecasts, 2021- 2033
4.3.5 Phase IV
4.3.5.1 Phase IV market estimates and forecasts, 2021- 2033
Chapter 5 Pharmacovigilance Market: Service Provider Estimates & Trend Analysis
5.1 Service provider Market Share Analysis, 2023 & 2030
5.2 Service Provider Dashboard
5.3 Market definition and scope
5.3.1 IN HOUSE
5.3.1.1 In house market estimates and forecasts, 2021- 2033
5.3.2 Contract Outsourcing
5.3.2.1 Contract outsourcing market estimates and forecasts, 2021- 2033
Chapter 6 Pharmacovigilance Market: Type Estimates & Trend Analysis
6.1 Type Market Share Analysis, 2023 & 2030
6.2 Type Dashboard
6.3 Market definition and scope
6.3.1 Spontaneous Reporting
6.3.1.1 Spontaneous Reporting market estimates and forecasts, 2021- 2033
6.3.2 Intensified ADR Reporting
6.3.2.1 Intensified ADR Reporting market estimates and forecasts, 2021- 2033
6.3.3 Targeted Spontaneous Reporting
6.3.3.1 Targeted spontaneous reporting market estimates and forecasts, 2021- 2033
6.3.4 Cohort Event Monitoring (CEM)
6.3.4.1 CEM market estimates and forecasts, 2021- 2033
6.3.5 EHR Mining
6.3.5.1 EHR Mining market estimates and forecasts, 2021- 2033
Chapter 7 Pharmacovigilance Market: Process Flow Estimates & Trend Analysis
7.1 Process Flow Market Share Analysis, 2023 & 2030
7.2 Process Flow Dashboard
7.3 Market definition and scope
7.3.1 Case Data Management
7.3.1.1 Case data management market estimates and forecasts, 2021- 2033
7.3.1.1.1 Case logging
7.3.1.1.1.1 Case logging market estimates and forecasts, 2021- 2033
7.3.1.1.2 Case data analysis
7.3.1.1.2.1 Case data analysis market estimates and forecasts, 2021- 2033
7.3.1.1.3 Medical reviewing and reporting
7.3.1.1.3.1 Medical reviewing and reporting market estimates and forecasts, 2021- 2033
7.3.2 Signal Detection
7.3.2.1 Signal detection market estimates and forecasts, 2021- 2033
7.3.2.1.1 Adverse event logging
7.3.2.1.1.1 Adverse Event Logging market estimates and forecasts, 2021- 2033
7.3.2.1.2 Adverse Event Analysis
7.3.2.1.2.1 Adverse Event Analysis market estimates and forecasts, 2021- 2033
7.3.2.1.3 Adverse Event Review & Reporting
7.3.2.1.3.1 Adverse Event Review & Reporting market estimates and forecasts, 2021- 2033
7.3.3 Risk Management System
7.3.3.1 Risk Management System market estimates and forecasts, 2021- 2033
7.3.3.1.1 Risk Evaluation System
7.3.3.1.1.1 Risk Evaluation System market estimates and forecasts, 2021- 2033
7.3.3.1.2 Risk Mitigation System
7.3.2.1.2.1 Risk Mitigation System market estimates and forecasts, 2021- 2033
Chapter 8 Pharmacovigilance Market: Therapeutic Area Estimates & Trend Analysis
8.1 Therapeutic Area Market Share Analysis, 2023 & 2030
8.2 Therapeutic Area Dashboard
8.3 Market definition and scope
8.3.1 Oncology
8.3.1.1 Oncology market estimates and forecasts, 2021- 2033
8.3.2 Neurology
8.3.2.1 Neurology market estimates and forecasts, 2021- 2033
8.3.3 Cardiology
8.3.3.1 Cardiology market estimates and forecasts, 2021- 2033
8.3.4 Respiratory Systems
8.3.4.1 Respiratory systems market estimates and forecasts, 2021- 2033
8.3.5 Others
8.3.5.1 Others market estimates and forecasts, 2021- 2033
Chapter 9 Pharmacovigilance Market: End Use Estimates & Trend Analysis
9.1 End Use Market Share Analysis, 2023 & 2030
9.2 End Use Dashboard
9.3 Market definition and scope
9.3.1 Pharmaceuticals
9.3.1.1 Pharmaceuticals market estimates and forecasts, 2021- 2033
9.3.2 Biotechnology Companies
9.3.2.1 Biotechnology companies market estimates and forecasts, 2021- 2033
9.3.3 Medical Device Manufacturers
9.3.3.1 Medical Device Manufacturers market estimates and forecasts, 2021- 2033
9.3.4 Others
9.3.4.1 Others market estimates and forecasts, 2021- 2033
Chapter 10 Pharmacovigilance Market: Regional Estimates & Trend Analysis, By, Product, Service Providers, Type, and End Use
10.1 Regional Market Snapshot
10.2 North America
10.2.1 North America Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.2.2 U.S.
10.2.2.1 U.S. Pharmacovigilance market estimates and forecasts, 2021- 2033
10.2.2.2 Competitive scenario
10.2.2.3 Regulatory Framework
10.2.3 Canada
10.2.3.1 Canada Pharmacovigilance market estimates and Forecasts, 2021- 2033
10.2.3.2 Competitive scenario
10.2.3.3 Regulatory Framework
10.3 Europe
10.3.1 Europe Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.3.2 UK
10.3.2.1 UK Pharmacovigilance market estimates and Forecasts, 2021- 2033
10.3.2.2 Competitive scenario
10.3.2.3 Regulatory Framework
10.3.3 Germany
10.3.3.1 Germany Pharmacovigilance market estimates and forecasts, 2018 - 2030 (USD Million
10.3.3.2 Competitive scenario
10.3.3.3 Regulatory Framework
10.3.4 France
10.3.4.1 France Pharmacovigilance market estimates and forecasts, 2021- 2033
10.3.4.2 Competitive scenario
10.3.4.3 Regulatory Framework
10.3.5 Italy
10.3.5.1 Italy Pharmacovigilance market estimates and forecasts, 2021- 2033
10.3.5.2 Competitive scenario
10.3.5.3 Regulatory Framework
10.3.6 Spain
10.3.6.1 Spain pharmacovigilance market estimates and forecasts, 2021- 2033
10.3.6.2 Competitive scenario
10.3.6.3 Regulatory Framework
10.3.7 Russia
10.3.7.1 Russia Pharmacovigilance market estimates and forecasts, 2021- 2033
10.3.7.2 Competitive scenario
10.3.7.3 Regulatory Framework
10.3.8 Denmark
10.3.8.1 Denmark Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.3.8.2 Competitive scenario
10.3.8.3 Regulatory Framework
10.3.9 Norway
10.3.9.1 Norway Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.3.9.2 Competitive scenario
10.3.9.3 Regulatory Framework
10.3.10 Sweden
10.3.10.1 Sweden Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.3.10.2 Competitive scenario
10.3.10.3 Regulatory Framework
10.4 Asia Pacific
10.4.1 Asia Pacific Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.4.2 JAPAN
10.4.2.1 Japan Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.4.2.2 Competitive scenario
10.4.2.3 Regulatory Framework
10.4.3 CHINA
10.4.3.1 China Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.4.3.2 Competitive Scenario
10.4.3.3 Regulatory Framework
10.4.4 India
10.4.4.1 India Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.4.4.2 Competitive Scenario
10.4.4.3 Regulatory Framework
10.4.5 Australia
10.4.5.1 Australia Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.4.5.2 Competitive Scenario
10.4.5.3 Regulatory Framework
10.4.6 Thailand
10.4.6.1 Thailand Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.4.6.2 Competitive Scenario
10.4.6.3 Regulatory Framework
10.4.7 South Korea
10.4.7.1 South Korea Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.4.7.2 Competitive Scenario
10.4.7.3 Regulatory Framework
10.5 Latin America
10.5.1 Latin America Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.5.2 Brazil
10.5.2.1 Brazil Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.5.2.2 Competitive Scenario
10.5.2.3 Regulatory Framework
10.5.3 Mexico
10.5.3.1 Mexico Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.5.3.2 Competitive Scenario
10.5.3.3 Regulatory Framework
10.5.4 Argentina
10.5.4.1 Argentina Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.5.4.2 Competitive Scenario
10.5.4.3 Regulatory Framework
10.6 MEA
10.6.1 MEA Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.6.2 South Africa
10.6.2.1 South Africa Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.6.2.2 Competitive Scenario
10.6.2.3 Regulatory Framework
10.6.3 Saudi Arabia
10.6.3.1 Saudi Arabia Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.6.3.2 Competitive Scenario
10.6.3.3 Regulatory Framework
10.6.4 UAE
10.6.4.1 UAE Arabia Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.6.4.2 Competitive Scenario
10.6.4.3 Regulatory Framework
10.6.5 Kuwait
10.6.5.1 Kuwait Pharmacovigilance Market Estimates and Forecasts, 2021- 2033
10.6.5.2 Competitive Scenario
10.6.5.3 Regulatory Framework
Chapter 11 Pharmacovigilance Market: Competitive Analysis
11.1 Market Participation Categorization
11.2 Public Companies
11.2.1 Company Market Position Analysis
11.2.2 Company Market Share
11.3 Private Companies
11.3.1 List of Key Emerging Companies
11.4 Competitive Factors and Strategies
11.4.1 Increasing strategic collaborations and product launch
11.4.2 Strategic Government initiatives which include collaborations
11.4.3 Competitors increased PV awareness program
11.4.4 Competitors increased collaboration and outsourcing of operations
11.4.5 Consolidation Trends
11.5 Healthcare Companies Using Pharmacovigilance Services
11.5.1 Potential Customers
11.5.2 Notable Cases
11.5.2.1 Case Study 1
11.5.2.1.1 Case Study 1
11.5.3.1.2 Case Study 2
11.5.2.2 Case Study 2
11.5.2.3 Case Study 3
11.5.3.4 Case Study 4
11.5.3 Key Focus areas for the pharmaceutical/healthcare companies
11.5.3.1 Adoption of technological advancements in life sciences industry
11.5.3.2 Published survey insights - related to adoption of pharmacovigilance automation
Chapter 12 Competitive Landscape
12.1 Company Profiles
12.1.1 ACCENTURE
12.1.1.1 Company overview
12.1.1.2 Service benchmarking
12.1.1.3 Financial performance
12.1.1.4 Strategic initiatives
12.1.1.5 SWOT Analysis
12.1.2 CLINQUEST GROUP B.V. (LINICAL AMERICAS)
12.1.2.1 Company overview
12.1.2.2 Service benchmarking
12.1.2.3 Financial performance
12.1.2.4 Strategic initiatives
12.1.2.5 SWOT Analysis
12.1.3 IQVIA Inc.
12.1.3.1 Company overview
12.1.3.2 Service benchmarking
12.1.3.3 Financial performance
12.1.3.4 Strategic initiatives
12.1.3.5 SWOT Analysis
12.1.4 COGNIZANT
12.1.4.1 Company overview
12.1.4.2 Service benchmarking
12.1.4.3 Financial performance
12.1.4.4 Strategic initiatives
12.1.4.5 SWOT Analysis
12.1.5 LABORATORY CORPORATION OF AMERICA HOLDINGS
12.1.5.1 Company overview
12.1.5.2 Service benchmarking
12.1.5.3 Financial performance
12.1.5.4 Strategic initiatives
12.1.5.5 SWOT Analysis
12.1.6 IBM
12.1.6.1 Company overview
12.1.6.2 Service benchmarking
12.1.6.3 Financial performance
12.1.6.4 Strategic initiatives
12.1.6.5 SWOT Analysis
12.1.7 ARISGLOBAL
12.1.7.1 Company Overview
12.1.7.2 Service Benchmarking
12.1.7.3 Financial Performance
12.1.7.4 Strategic Initiatives
12.1.7.5 SWOT Analysis
12.1.8 ICON PLC.
12.1.8.1 Company Overview
12.1.8.2 Service Benchmarking
12.1.8.3 Financial Performance
12.1.8.4 Strategic Initiatives
12.1.8.5 SWOT Analysis
12.1.9 CAPGEMINI
12.1.9.1 Company Overview
12.1.9.2 Service Benchmarking
12.1.9.3 Financial Performance
12.1.9.4 Strategic Initiatives
12.1.9.5 SWOT Analysis
12.1.10 ITCLINICAL
12.1.10.1 Company Overview
12.1.10.2 Service Benchmarking
12.1.10.3 Financial Performance
12.1.10.4 Strategic Initiatives
12.1.10.5 SWOT Analysis
12.1.11 TAKE SOLUTIONS LIMITED
12.1.11.1 Company Overview
12.1.11.2 Service Benchmarking
12.1.11.3 Financial Performance
12.1.11.4 Strategic Initiatives
12.1.11.5 SWOT Analysis
12.1.12 PAREXEL INTERNATIONAL CORPORATION.
12.1.12.1 Company Overview
12.1.12.2 Service Benchmarking
12.1.12.3 Financial Performance
12.1.12.4 Strategic Initiatives
12.1.12.5 SWOT Analysis
12.1.13 BIOCLINICA, INC.
12.1.13.1 Company overview
12.1.13.2 Service benchmarking
12.1.13.3 Financial performance
12.1.13.4 Strategic initiatives
12.1.13.5 SWOT Analysis
12.1.14 WIPRO
12.1.14.1 Company Overview
12.1.14.2 Service Benchmarking
12.1.14.3 Financial Performance
12.1.14.4 Strategic Initiatives
12.1.14.5 SWOT Analysis
12.1.15 UNITED BIOSOURCE LLC
12.1.15.1 Company Overview
12.1.15.2 Service Benchmarking
12.1.15.3 Financial Performance
12.1.15.4 Strategic initiatives
12.1.15.5 SWOT Analysis
12.1.16 FMD K&L (CLINCHOICE)
12.1.16.1 Company Overview
12.1.16.2 Service Benchmarking
12.1.16.3 Financial performance
12.1.16.4 Strategic initiatives
12.1.16.5 SWOT Analysis
Chapter 13 Winning Strategies
13.1 Key Winning/Scoring Criteria
13.1.1 By Categories
13.1.1.1 Pharmaceuticals
13.1.1.2 Biotech companies
13.1.1.3 Medical device companies
13.2 Key Vendor Selection Factors
13.2.1 By Category
13.2.2 By Company Size
13.2.2.1 Key Takeaways
Chapter 14 Switching Cost Analysis
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