The global molecular diagnostics market is estimated to be valued at USD 16.33 Billion in 2024 and is expected to reach USD 36.55 Billion by 2031, exhibiting a compound annual growth rate (CAGR) of 12.2% from 2024 to 2031.
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The increasing prevalence of infectious diseases and genetic disorders, technological advancements in molecular diagnostics, and growing application areas of polymerase chain reaction and next generation sequencing are driving the growth of this market.
Increasing prevalence of infectious diseases and cancer
The growing incidences of various infectious diseases such as HIV, hepatitis, tuberculosis as well as the rising cancer cases globally are propelling the demand for advanced molecular diagnostic techniques. Early detection of diseases has been proven to significantly increase the survival rates and chances of complete recovery. According to the WHO, tuberculosis remains one of the top 10 causes of death worldwide. While considerable progress has been made in diagnosing and treating the bacteria, conventional methods can often take weeks to confirm the infection. This creates a clear advantage for molecular diagnostic tests that can identify TB bacteria in a matter of hours from a simple sputum sample. Their high sensitivity allows for rapid detection of even drug-resistant strains, enabling physicians to begin the right treatment protocol without any delay. Similarly, cancer remains a leading cause of mortality even in developed countries. While advanced therapeutic measures have boosted overall cancer survival rates over the past few decades, most benefit is seen when the disease is identified at an early stage. Traditional diagnostics are not always adequate in detecting cancer at the cellular and molecular level in its early stages. Molecular testing examines genetic expressions and mutations to pinpoint the presence of malignancies with utmost accuracy. This helps determine the most suitable course of action, whether it be surgery, chemotherapy or a combination of treatment approaches. Timely diagnosis and intervention are critical in improving a patient's chances against the illness. With global cancer burden projected to rise further in the coming years, demand for reliable molecular tests from oncologists will continue growing at a rapid pace.
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Technological advancements in molecular diagnostics
The molecular diagnostics market has witnessed significant technological innovation which has expanded its applications manifolds. Next generation sequencing or NGS has revolutionized genomic analysis, allowing fast and comprehensive profiling of the entire DNA or RNA composition from a simple sample. With continuously declining costs, whole genome sequencing is being utilized for diagnostic discovery research and shifting early disease detection capabilities. Synthetic biology is enabling design of novel biomarker detection platforms. Advanced machine learning algorithms are also being deployed to analyze the voluminous data generated from these sequencing tests and simplify reporting for clinicians. All these cutting-edge innovations have made molecular analysis more powerful, convenient and affordable. Miniaturization of molecular diagnostic devices using microfluidics and nanotechnology has enhanced portability. Miniaturized PCR and genome sequencing panels integrated on a single microchip or cartridge are simplifying testing. Examples include handheld and portable genetic analyzers and mini-labs which can perform complex multistep molecular assays on location, delivering results within hours instead of days. This has important applications in decentralized healthcare settings, especially for infectious disease control in developing regions. Transition to automation is further improving productivity, reducing manual errors, and turnaround times. Integration of molecular diagnostics onto smartphones is also being extensively researched for creating truly point-of-care testing solutions.
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