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Global Pharmacovigilance and Drug Safety Software Market 2019-2023 to Post a CAGR of 6% Includes business research, Key players, Revenue Size & Share, Complete Industry Analysis | 360 Research Reports

Pharmacovigilance and Drug Safety Software

The data collected in the “Global Pharmacovigilance and Drug Safety Software Market – Segmented by Functionality, Mode of Delivery, End Users, and Geography – Growth, Trends, and Forecast (2019 – 2023)” report (Sample Copy Here) offers detailed insights on the market dynamic forces to enable informed business decision making and development strategy formulation supported on the opportunities present in the market. Pharmacovigilance and Drug Safety Software Market report delivers the most up-to-date industry data on the actual and potential market situation, and outlook.

The Global Pharmacovigilance and Drug Safety Software Market 2019 is bifurcated into multiple segments [Product, Applications, End-Users, and Major Regions]. The global Pharmacovigilance and Drug Safety Software Market report represents the market’s data in a better-analyzed way by fragmenting the market in several multiple segments product, its end-users, applications, and others of the market segments. A review of the impact of the administrative regulations and policies on the Pharmacovigilance and Drug Safety Software Market operations is also included in this report. The Pharmacovigilance and Drug Safety Software Market report offers a complete analysis of competitive dynamics that are modifying and places the patrons ahead of competitors.

Pharmacovigilance and Drug Safety Software Market Segmentation by Major Players:

Arisglobal, Ennov Solutions, Inc., Extedo Gmbh, Online Business Applications, Inc., Oracle Corporation, Sarjen Systems Pvt Ltd, Sparta Systems, Inc., United Biosource Corporation, Ab Cube, Umbra Global Llc.

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Overview of Pharmacovigilance and Drug Safety Software Market Report:

The global pharmacovigilance and drug safety software market is projected to witness a CAGR of 6% during the forecast period of 2019–2023.

Increasing Incidences of Adverse Drug Reactions (ADRs)

Adverse drug reaction (ADR) refers to injuries arising from the consumption of medication. ADR may arise due to a single dose of the medication or may manifest after prolonged exposure. ADR can also arise due to the interaction between two or more drug substances consumed simultaneously or in quick succession. ADRs cause considerable mortality and morbidity worldwide. According to research estimates, approximately 5% of all hospital admissions in Europe are caused by ADRs. Additionally, there is a high incidence rate of ADR among hospitalized patients. Pharmacovigilance assumes great importance in such settings. The World Health Organization (WHO), in 1971, devised an international system for monitoring adverse reactions to drugs by using information derived from member states. The global database for ADRs is maintained by Uppsala Monitoring Centre (UMC), based in Sweden. The database contains reports of suspected ADRs, so-called Individual Case Safety Reports (ICSRs), and collected by national drug authorities in over 110 countries spanning over more than 100,000 different medicinal products. The extensive nature of this database is indicative of the myriad of ADR cases that arise globally and need to be monitored for mitigating future incidences. Thus, the increasing incidence of ADRs is driving the growth of global pharmacovigilance and drug safety software market. Apart from these, factors, like increasing adoption of pharmacovigilance software by outsourcing companies involved in contract research and contract manufacturing, and government policies pertaining to drug safety regulation are driving the growth of this market.

Lack of Pharmacovigilance Professionals

Healthcare professionals play a crucial role in the pharmacovigilance system. Professionals in this field are required to possess considerable knowledge and expertise in the field of medication safety to successfully contribute to this area through early recognition, management, and reporting of the medicine safety issues. Furthermore, the healthcare professionals should be well educated about the necessity and procedure of adverse event reporting. They should possess a combination of training and research skills in this area. Despite global concerns against medication safety, there is a lack of awareness and knowledge of pharmacovigilance and ADR reporting among healthcare professionals. Moreover, recent studies have indicated that ADRs are poorly reported by healthcare providers, especially in developing countries. Consequently, the lack of pharmacovigilance professionals inhibits the growth of this market. Further, the lack of standard regulations in adverse drug reaction reporting is restraining the growth of this market.

Drug Safety Audits Software Leads the Market Segment

By functionality, the pharmacovigilance and drug safety software market has been segmented into adverse event reporting software, drug safety audits software, issue tracking software, and fully integrated software. Based on recent trends the fully integrated software category is the fastest growing category, but the market leader in the segment is drug safety audits software. Its high market share is attributed to the increasing number of contract research and manufacturing organizations, which are making extensive use of safety audits for ensuring compliance with standards set by apex drug regulatory bodies.

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Reasons to Purchase the Report

  • Follow the current and future pharmacovigilance and drug safety software market in the developed and emerging markets.
  • Analyzing various perspectives of the market with the help of Porter’s Five Forces Analysis.
  • Identify the segment that is expected to dominate the market.
  • Identify the regions that are expected to witness the fastest growth during the forecast period.
  • Identify the latest developments, market shares, and strategies employed by the major market players.
  • 3 month analyst support along with the Market Estimate sheet (in Excel).

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    Further, in the Pharmacovigilance and Drug Safety Software Market research reports, the following points are included along with an in-depth study of each point:

    Production Analysis – Production of the Pharmacovigilance and Drug Safety Software is analyzed with respect to different regions, types, and applications. Here, price analysis of various Pharmacovigilance and Drug Safety Software Market key companies is also covered.

    Competitors – In this section, various Pharmacovigilance and Drug Safety Software industry-leading players are studied with respect to their company profile, product portfolio, capacity, price, cost, and revenue.

    Sales and Revenue Analysis – Both, sales and revenue are studied for the different regions of the Pharmacovigilance and Drug Safety Software Market. Another major aspect, price, which plays an important part in the revenue generation, is also measured in this section for the numerous regions.

    Supply and Consumption – In continuation with sales, this section studies supply and consumption for the Pharmacovigilance and Drug Safety Software Market. This part also shelters light on the gap between supply and consumption. Import and export statistics are also given in this part.

    Other analyses – Apart from the above-mentioned information, trade and distribution analysis for the Pharmacovigilance and Drug Safety Software Market, the contact information of major manufacturers, suppliers and key consumers is also given. In addition, SWOT analysis for new projects and viability analysis for new investment are included.

     “We also can offer a customized report to fulfill the special requirements of our clients. Regional and Countries report can be provided as well.”

    Lastly, with a team of vivacious industry professionals, we offer our clients with high-value market research that, in turn, would aid them to decipher new market avenues together with new strategies to take hold of the market share.

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