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Global Drug Safety Solutions and Pharmacovigilance Market, By Type (Software, Services), Product (Standard Form, Customized Form), Functionality (Adverse Event Reporting Software, Drug Safety Audits Software, Issue Tracking Software), Delivery (On-Premise Delivery Mode, On-Demand/Cloud-Based (SAAS) Delivery Mode), End Users (Biotechnology and Pharmaceuticals, Contract Research Organizations (CROS), Hospitals, KPOs/BPOs, Healthcare Providers), Distribution Channel (Direct Sales, Retail Sales) u2013 Industry Trends and Forecast to 2030.<br><br>
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Global Drug Safety Solutions and Pharmacovigilance Market – Industry Trends and Forecast to 2030 The rising prevalence of adverse drug reactions (ADRs) is the primary driver of the drug safety solutions and pharmacovigilance market. Furthermore, the increasing adoption of pharmacovigilance software by outsourcing companies and strict government regulations for drug prior and post-commercialization contribute to the market's overall growth. The market is expected to benefit from research collaborations and partnerships, as well as drug safety solutions and pharmacovigilance automation, which aid in achieving more effective and durable mechanical hemostasis. Data Bridge Market Research analyses that the drug safety solutions and pharmacovigilance market which was USD 7.8 billion in 2022, is expected to reach USD 13.91 billion by 2030, at a CAGR of 7.50% during the forecast period 2023 to 2030. In addition to the insights on market scenarios such as market value, growth rate, segmentation, geographical coverage, and major players, the market reports curated by the Data Bridge Market Research also include depth expert analysis, patient epidemiology, pipeline analysis, pricing analysis, and regulatory framework. https://www.databridgemarketresearch.com/reports/global-drug-safety-solutions-and-pharmacovigilance-market
Report Description Market Definition Drug safety and pharmacovigilance (PV or PHV) is a scientific procedure for collecting, analyzing, monitoring, and preventing adverse effects in drugs and therapies. Its primary goal is to ensure that pharmaceutical developers meet industry regulatory standards, and it puts additional pressure on biotechnology and pharmaceutical companies to manufacture safe drugs and evaluate their post-sales results. Drug Safety Solutions and Pharmacovigilance Market Dynamics Drivers Rising regulatory mandates on clinical trials Regulatory mandates on clinical trial conduct and post-marketing vigilance are driving the demand for PV services. For instance, the European Medicines Agency (EMA) and the United States Food and Drug Administration (FDA) develop regulatory guidelines for all stages of clinical trials. Advances in the development of ADR databases and information systems enabled the reporting of accurate information, which research professionals can then use for prospective studies, thereby fuelling overall demand. https://www.databridgemarketresearch.com/reports/global-drug-safety-solutions-and-pharmacovigilance-market
Market Overview Opportunities Growing R&D activities Increasing R&D and adopting new technologies in clinical research also contribute to market growth. For instance, the incorporation of virtual services into clinical trial protocols by market players such as IQVIA and PRA Health Sciences is expected to drive demand in the coming years. Restraints/Challenges Rising complexity related to drug safety regulations The increasing complexity related to drug safety regulations and misquoting and miscoding of adverse actions pose a challenge for the market’s growth. Recent Developments In 2019, The Laboratory Corporation of America Health EC and The New Jersey announced a collaboration and the development of a database and information exchange platform. This platform will be beneficial in conjunction with LabCorp's Care Intelligence application. This collaboration will result in better lives and health for LabCorp employees. This will result in increased patient satisfaction and recognition. In 2019, Parexel International Corporation announced that they had formed a strategic partnership with Datavant, Inc. to connect real-world data, including all clinical trials conducted by Parexel. This collaboration will broaden and extend the company's entire portfolio, making data linking available to more customers. https://www.databridgemarketresearch.com/reports/global-drug-safety-solutions-and-pharmacovigilance-market
Key Players • Some of the major players operating in the drug safety solutions and pharmacovigilance market are: • PPD Inc (U.S.) • Drug Safety Solutions Limited (U.S.) • C3i (U.S.) • Worldwide Clinical Trials (U.S.) • Bioclinica (U.S.) • United Biosource LLC (U.S.) • Ennov (Hong Kong) • AB Cube S.A.S. (France) • Labcorp Drug Development (U.S.) • Accenture (Ireland) • ICON plc (U.S.) • Ergomed plc (U.K.) • IQVIA (U.S.) • Genpact (U.S.) • Cognizant (U.S.) • Parexel International Corporation (U.S.) • ArisGlobal (U.S.) https://www.databridgemarketresearch.com/reports/global-drug-safety-solutions-and-pharmacovigilance-market
About Data Bridge Market Research An absolute way to forecast what future holds is to comprehend the trend today! Data Bridge Market Research set forth itself as an unconventional and neoteric Market research and consulting firm with unparalleled level of resilience and integrated approaches. We are determined to unearth the best market opportunities and foster efficient information for your business to thrive in the market. Contact Us:- Data Bridge Market Research US: +1 888 387 2818 UK: +44 208 089 1725 Hong Kong: +852 8192 7475 Email:- corporatesales@databridgemarketresearch.com