The global compound management market is estimated to be valued at USD 501.2 Mn in 2025 and is expected to reach USD 1,326.0 Mn by 2032, exhibiting a compound annual growth rate (CAGR) of 14.9% from 2025 to 2032. The market is witnessing significant growth owing to the rising drug discovery activities and the growing need for efficient sample management in pharmaceutical and biotechnology industries.
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Increasing R&D expenditure by pharmaceutical companies
The global pharmaceutical industry has been witnessing significant investments in research and development over the past few years. While drugs go off-patent and competition intensifies, large pharmaceutical companies are making substantial R&D investments to bring novel therapies to the market. They are exploring new treatment areas and disease pathways through extensive clinical research activities. Continuous development of innovative drug candidates requires efficient management of large chemical libraries and biological sample collections. Pharmaceutical companies are realizing the need for specialized platforms and skilled professionals to properly store, track, retrieve, and distribute compounds and samples involved in various stages of drug discovery and development. This ensures smooth progress of research projects by having desired materials readily available when needed.
Centralized compound management services provide pharmaceutical research organizations the advantage of outsourcing the tasks related to receipt, inventory, storage, and dispensing of research materials. This allows them to focus internal resources on core scientific activities rather than allocating time and money on non-core operational aspects. Such specialized third-party service providers have sophisticated infrastructures and expert personnel to appropriately handle the logistical challenges of compound management. Their automated, standardized processes help maintain sample integrity throughout complex research undertakings. This gives confidence to pharmaceutical companies that valuable research inputs and outputs are protected against any risks of loss, cross-contamination or non-compliance issues. As drug development scales to higher volumes due to open innovation models as well, the demand for reliable compound management is surging in the industry.
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