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Mass Spectrometry Market

Pages: 140 | Base Year: 2024 | Release: June 2025 | Author: Sunanda G.

Market Definition

Mass spectrometry (MS) includes analytical instruments that measure the mass-to-charge ratios of ions to identify and quantify molecules with high precision. These systems drive discovery and innovation in chemistry, biochemistry, environmental science, and pharmaceuticals. 

The market supports a broad range of applications including drug development, proteomics, forensic analysis, and environmental monitoring by delivering accurate molecular insights.

Mass Spectrometry Market Overview

The global mass spectrometry market size was valued at USD 6,271.6 million in 2024 and is projected to grow from USD 6,660.4 million in 2025 to USD 10,778.1 million by 2032, exhibiting a CAGR of 7.12% during the forecast period. 

The market is growing due to the increasing use of mass spectrometry in clinical diagnostics and personalized medicine, where precise molecular analysis is essential for biomarker discovery and therapeutic monitoring. Additionally, the development of miniaturized and portable MS systems is expanding on-site testing applications in environmental, forensic, and food safety sectors.

Major companies operating in the mass spectrometry industry are Thermo Fisher Scientific Inc., Agilent Technologies, Inc., Danaher Corporation, Waters Corporation, Bruker, Shimadzu Corporation, PerkinElmer, F. Hoffmann-La Roche Ltd, Analytik Jena GmbH+Co. KG, Elementar Analysensysteme GmbH, Hiden Analytical, Hitachi, Ltd., MKS Inc., Rigaku Holdings Corporation, and LECO Corporation.

The surge in pharmaceutical and biotechnology research and development activities is driving significant demand for mass spectrometry technologies.

  • In January 2025, the Department of Biotechnology completed the first phase of the Genome India Project. It unveiled a new platform and framework for sharing a dataset comprising 10,000 genome sequences from healthy individuals across 99 ethnic groups and establishing a baseline map of India’s genetic diversity.

Mass spectrometry plays a critical role in drug discovery, quality control, proteomics, and metabolomics by enabling precise molecular analysis. Increasing focus on developing targeted therapies and biologics requires highly sensitive and accurate analytical instruments. 

Pharmaceutical companies are relying on mass spectrometry to ensure regulatory compliance, validate drug formulations, and detect impurities during manufacturing. Expanding research into disease biomarkers and personalized medicine is further elevating the use of mass spectrometry in life sciences.

Mass Spectrometry Market Size & Share, By Revenue, 2025-2032

Key Highlights

  1. The mass spectrometry market size was valued at USD 6,271.6 million in 2024.
  2. The market is projected to grow at a CAGR of 7.12% from 2025 to 2032.
  3. North America held a market share of 36.42% in 2024, with a valuation of USD 2,284.1 million.
  4. The instruments segment garnered USD 3,525.3 million in revenue in 2024.
  5. The pharmaceuticals and biotechnology segment is expected to reach USD 3,101.2 million by 2032.
  6. Asia Pacific is anticipated to grow at a CAGR of 8.08% during the forecast period.

Market Driver

Clinical Diagnostics and Personalized Medicine Growth

The growing adoption of mass spectrometry in clinical diagnostics is driving the expansion of personalized medicine and accelerating the growth of the market. Clinical laboratories are increasingly using mass spectrometry for detecting biomarkers, monitoring therapeutic drug levels, and identifying complex disease profiles with high accuracy. 

Demand for personalized healthcare solutions is prompting the use of advanced analytical tools that provide precise and patient-specific data. Healthcare providers are utilizing mass spectrometry to improve diagnostic accuracy, enable early disease detection, and tailor treatment plans based on individual molecular signatures. Integration of mass spectrometry into routine clinical workflows is enhancing efficiency and diagnostic confidence.

  • In December 2024, Roche launched the cobas Mass Spec solution including the cobas i 601 analyzer and the Ionify reagent pack covering four assays for steroid hormones. The system delivers a fully automated, integrated, and standardized workflow for clinical mass spectrometry. It supports over 60 analytes across steroid hormones, vitamin D, immunosuppressant drugs, therapeutic drug monitoring, and drugs of abuse testing.

Market Challenge

High Capital and Operational Costs

A key challenge in the mass spectrometry market is dealing with high capital investments required for equipment purchase and ongoing operational costs. 

Premium pricing of instruments, along with expensive maintenance services and consumables, are making it difficult for smaller laboratories to afford and sustain these technologies. This cost barrier is limiting widespread adoption across academic, clinical, and small-scale research settings.

To address this challenge, market players are offering leasing options, bundled service packages, and entry-level models that lower the financial threshold. Companies are also enhancing instrument durability and simplifying maintenance procedures to reduce long-term ownership costs.

Market Trend

Miniaturization & Portable MS Systems

A major trend in the market is the development of miniaturized and portable systems designed for field deployment. Researchers and manufacturers are utilizing microfluidics and ambient ionization techniques to create compact instruments capable of performing complex analyses outside traditional laboratory settings. 

These advancements are enabling rapid on-site testing in environmental monitoring, forensic investigations, and food safety assessments. Portability is reducing turnaround times and allowing immediate decision-making in critical applications. Lightweight designs and simplified interfaces make these systems easily accessible to non-specialist users in diverse field environments.

  • In June 2023, BaySpec launched the portability miniature portable mass spectrometer. This compact instrument weighs approximately 10 kg and supports ambient ionization techniques such as ESI and APCI for real-time analysis of vapors, liquids, and solids. Device users can perform complex analyses in the field without sample preparation or laboratory infrastructure.

Mass Spectrometry Market Report Snapshot

Segmentation

Details

By Product Type

Instruments, Consumables & Services

By Application

Omics Research, Pharmaceuticals and Biotechnology, Clinical Diagnostics, Environmental Testing, Food and Beverage Testing, Others

By Region

North America: U.S., Canada, Mexico

Europe: France, UK, Spain, Germany, Italy, Russia, Rest of Europe

Asia-Pacific: China, Japan, India, Australia, ASEAN, South Korea, Rest of Asia-Pacific

Middle East & Africa: Turkey, U.A.E., Saudi Arabia, South Africa, Rest of Middle East & Africa

South America: Brazil, Argentina, Rest of South America

Market Segmentation

  • By Product Type (Instruments and Consumables & Services,): The instruments segment earned USD 3,525.3 million in 2024, due to the consistent demand for high-performance analytical systems in pharmaceutical quality control, clinical diagnostics, and research applications.
  • By Application (Omics Research, Pharmaceuticals and Biotechnology, Clinical Diagnostics, Environmental Testing, Food and Beverage Testing, and Others): The pharmaceuticals and biotechnology segment held 32.85% of the market in 2024, owing to its widespread use in drug development, quality control, and biologics characterization.

Mass Spectrometry Market Regional Analysis

Based on region, the global market has been classified into North America, Europe, Asia Pacific, Middle East & Africa, and South America.

Mass Spectrometry Market Size & Share, By Region, 2025-2032

The North America mass spectrometry market share stood at 36.42% in 2024, with a valuation of USD 2,284.1 million. This dominance is attributed to the growing focus of pharmaceutical and biotechnology companies in North America on developing biologics, biosimilar, and gene therapies. 

These advanced therapeutics demand precise analytical tools to ensure molecular integrity and maintain batch-to-batch consistency. Mass spectrometry plays a vital role in the drug development and manufacturing process by enabling the detailed characterization of large molecules, detecting impurities, and validating drug formulations, positioning it as a critical technology in biologics manufacturing.

  • In June 2024, BioPharmaSpec, a US-based CRO specializing in biologics and gene therapies, announced the purchase of a suite of advanced mass spectrometry instruments, including the Waters Select Series CYCLIC Ion Mobility LCMS/MS, SCIEX ZenoTOF 7600 LCMS/MS, Waters Xevo TQ Absolute, and Waters Xevo G3 LCMS/MS Q‑. Instrumentation was added to support the preclinical characterization of biologics, biosimilars, monoclonal antibodies, antibody–drug conjugates, peptides, oligonucleotides, and AAVbased gene therapies.

Asia Pacific is poised for significant growth at a CAGR of 8.08% over the forecast period, owing to the region’s emergence as a global hub for pharmaceutical manufacturing, with a rising number of companies engaged in formulation development, generics, and contract manufacturing. 

To comply with international quality standards and regulatory guidelines, these companies are increasingly adopting advanced analytical technologies such as mass spectrometry. Widely used for impurity profiling, stability testing, and quality assurance, mass spectrometry plays a critical role in supporting the region’s expanding pharmaceutical production capabilities.

Regulatory Frameworks

  • In the U.S., the Food and Drug Administration (FDA) regulates mass spectrometry used in clinical settings as Class II medical devices, requiring 510(k) clearance under the Federal Food, Drug, and Cosmetic Act. The United States Pharmacopeia (USP) also mandates MS-based methods for impurity detection in biologics. For pharmaceutical use, MS methods must comply with FDA’s analytical method validation guidelines and Good Laboratory Practice (GLP) requirements enforced by the Environmental Protection Agency (EPA).
  • In Europe, mass spectrometry instruments used in diagnostics fall under the In Vitro Diagnostic Regulation (IVDR – Regulation EU 2017/746), requiring conformity assessment and CE marking. In pharmaceutical quality control, methods must comply with the European Medicines Agency’s EudraLex Volume 4 Good Manufacturing Practice (GMP) standards and European Pharmacopoeia (Ph. Eur.). Chemical testing must follow the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and Classification, Labelling and Packaging (CLP) regulations.
  • In China, the National Medical Products Administration (NMPA) regulates the use of mass spectrometry in clinical diagnostics and pharmaceutical applications under China's GMP and GLP frameworks. Diagnostic instruments must meet in vitro diagnostic (IVD) standards aligned with international norms.
  • Japan regulates mass spectrometry through the Pharmaceuticals and Medical Devices Agency (PMDA) and the Ministry of Health, Labour and Welfare (MHLW), following Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) guidelines in line with the International Council for Harmonisation (ICH). Clinical applications of MS must comply with IVD rules under Japan’s Pharmaceutical and Medical Device Act.

Competitive Landscape

Major players in the mass spectrometry market are adopting strategies such as product innovation, research and development, and strategic partnerships to strengthen their position and support market growth. 

Several companies are focused on launching high-performance instruments that offer greater speed, sensitivity, and resolution to meet the evolving needs of proteomics and biopharmaceutical research. Collaboration with academic institutions and pharmaceutical companies is helping manufacturers enhance their application capabilities and expand their customer base in clinical and research settings.

  • In June 2025, Thermo Fisher Scientific launched the Orbitrap Astral Zoom and Orbitrap Excedion Pro mass spectrometers. The new instruments deliver enhanced speed, sensitivity, and resolution for proteomics and biopharmaceutical research.

List of Key Companies in Mass Spectrometry Market:

  • Thermo Fisher Scientific Inc. 
  • Agilent Technologies, Inc.
  • Danaher Corporation
  • Waters Corporation
  • Bruker
  • Shimadzu Corporation
  • PerkinElmer
  • Hoffmann-La Roche Ltd
  • Analytik Jena GmbH+Co. KG
  • Elementar Analysensysteme GmbH
  • Hiden Analytical
  • Hitachi, Ltd.
  • MKS Inc.
  • Rigaku Holdings Corporation
  • LECO Corporation

Recent Developments (Partnership/Product Launches)

  • In December 2024, Roche introduced the cobas Mass Spec solution. The CE-marked package, comprising the cobas i 601 analyser and Ionify reagent assays enables automated clinical mass spectrometry testing across more than 60 analytes.
  • In June 2024, Waters Corporation launched the Xevo MRT mass spectrometer. The multi-reflecting time-of-flight system provides high-resolution analysis while promoting sustainability at ASMS 2024.
  • In May 2024, SepSolve Analytical partnered with HyperChrom SA. The partnership combines HyperChrom’s fast gas chromatography tools with SepSolve’s BenchTOF2 time-of-flight mass spectrometer for enhanced analytical workflows.
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