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Pharmacovigilance and Drug Safety Software Market size was valued at USD 171.7 million in 2022 and is estimated to grow at a CAGR of 6.6% to reach USD 319.9 million by 2032 attributed to the rising number of adverse drug reactions (ADRs) that has increased the need for reliable and efficient pharmacovigilance and drug safety software use
Stringent guidelines by government and regulatory bodies have increased the adoption of pharmacovigilance and drug safety software for drug safety monitoring, signal detection, and risk management. Also, increasing number of drug development and clinical trials has further soared the demand for pharmacovigilance and drug safety software by pharmaceutical companies to effectively monitor the safety profiles of drugs in development and during clinical trials. Further, the adoption of artificial intelligence and machine learning in pharmacovigilance software has proven instrumental in streamlining the process of identifying potential safety issues and improving patient outcomes.
Report Attribute | Details |
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Base Year: | 2022 |
Pharmacovigilance and Drug Safety Software Market Size in 2022: | USD 171.7 Million |
Forecast Period: | 2023 to 2032 |
Forecast Period 2023 to 2032 CAGR: | 6.6% |
2032 Value Projection: | USD 319.9 Million |
Historical Data for: | 2018 to 2022 |
No. of Pages: | 118 |
Tables, Charts & Figures: | 211 |
Segments covered: | Functionality, Mode of Delivery, End-use, and Region |
Growth Drivers: |
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Pitfalls & Challenges: |
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Pharmacovigilance and drug safety software are tools used by pharmaceutical companies, regulatory agencies, and healthcare organizations to monitor, track, and manage the safety and effectiveness of drugs and other medical products. These software systems play a crucial role in the process of pharmacovigilance, which involves the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems.