Non-invasive Prenatal Testing Market Outlook From USD 4.7 Bn in 2024 to USD 13.2 Bn by 2035 | TMR Report

Based on end-user, the global non-invasive prenatal testing market has been divided into hospitals, diagnostic laboratories, specialty clinics, and others.

WILMINGTON, DE, UNITED STATES, August 26, 2025 /EINPresswire.com/ -- The global Non-invasive Prenatal Testing (NIPT) market, valued at USD 4.7 billion in 2024, is projected to reach USD 13.2 billion by 2035, expanding at a CAGR of 9.5% from 2025 to 2035. This growth is driven by rising awareness of early genetic screening, advancements in genomic technologies, increasing maternal age, and the growing preference for safe, accurate, and non-invasive testing methods over traditional procedures.

Rising prevalence of Down syndrome cases and growing maternal age and associated chromosomal risks are driving the non-invasive prenatal testing market demand. Moreover, physicians are choosing advanced DNA-based screening methods like NIPT due to their high safety, accuracy, and early screening for chromosomal abnormalities in pregnancy.

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Non-invasive Prenatal Testing, or NIPT, is a test performed during pregnancy to asess the risk of certain genetic conditions in a fetus. It is performed by analysing small fragments of fetal DNA in the mother's blood, usually as early as week 10 of pregnancy. Unlike invasive procedures such as amniocentesis or chorionic villus sampling (CVS), NIPT is not harmful to the fetus in any way because it is just a routine blood test on the mother.

Compared to invasive testing procedures like amniocentesis with a risk of complications, NIPT is a non-invasive testing procedure that provides accurate findings, making it a procedure of choice among physicians and expectant couples alike.

𝗠𝗮𝗿𝗸𝗲𝘁 𝗦𝗲𝗴𝗺𝗲𝗻𝘁𝗮𝘁𝗶𝗼𝗻

𝗧𝗵𝗲 𝗡𝗜𝗣𝗧 𝗺𝗮𝗿𝗸𝗲𝘁 𝗰𝗮𝗻 𝗯𝗲 𝘀𝗲𝗴𝗺𝗲𝗻𝘁𝗲𝗱 𝗯𝗮𝘀𝗲𝗱 𝗼𝗻 𝘀𝗲𝘃𝗲𝗿𝗮𝗹 𝗸𝗲𝘆 𝗳𝗮𝗰𝘁𝗼𝗿𝘀:

𝗕𝘆 𝗦𝗲𝗿𝘃𝗶𝗰𝗲 𝗧𝘆𝗽𝗲:

Cell-Free DNA Screening: This is the largest and most dominant segment, as it's the core technology behind NIPT. It involves analyzing cfDNA from maternal blood to detect chromosomal abnormalities.

Biochemical Marker Screening: This involves analyzing specific proteins and hormones in the mother's blood to assess the risk of certain conditions. While less accurate than cfDNA, it's a complementary or alternative screening method.

Ultrasound Screening: This is another non-invasive method often used in conjunction with NIPT to screen for structural abnormalities.

By Sourcing Type:

In-house: Testing performed within a company's own laboratory.

Outsourced: Samples sent to a third-party diagnostic laboratory for analysis.

𝗕𝘆 𝗔𝗽𝗽𝗹𝗶𝗰𝗮𝘁𝗶𝗼𝗻:

Trisomy Detection: The largest application segment, primarily for screening Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13).

Microdeletion Screening: A growing segment for detecting smaller chromosomal deletions that can lead to various genetic disorders.

Sex Chromosome Aneuploidies: Screening for conditions like Turner syndrome and Klinefelter syndrome.

Other Applications: This includes screening for single-gene disorders, among other conditions.

𝗕𝘆 𝗜𝗻𝗱𝘂𝘀𝘁𝗿𝘆 𝗩𝗲𝗿𝘁𝗶𝗰𝗮𝗹/𝗘𝗻𝗱 𝗨𝘀𝗲𝗿:

Diagnostic Laboratories: The primary end-users, where the majority of NIPT tests are processed.

Hospitals and Birthing Centers: These facilities act as a primary point of contact for patient samples and counseling.

Research Institutes: These institutions are involved in developing new NIPT applications and technologies.

𝗕𝘆 𝗥𝗲𝗴𝗶𝗼𝗻:

North America: Dominates the market with the largest share, thanks to advanced healthcare infrastructure, high healthcare spending, and a strong presence of key market players. The US alone is a major hub for innovation and commercialization.

Europe: The second-largest market, with a significant push from government reimbursement policies in countries like the Netherlands and Germany, which have made NIPT a publicly funded option.

Asia Pacific: This region is projected to be the fastest-growing market, driven by a large patient population, rising disposable incomes, and increasing awareness of advanced prenatal care.

Latin America and the Middle East & Africa: These regions are also experiencing growth, albeit from a smaller base, due to improving healthcare infrastructure and growing awareness.

𝗥𝗲𝗴𝗶𝗼𝗻𝗮𝗹 𝗔𝗻𝗮𝗹𝘆𝘀𝗶𝘀

North America is expected to maintain its lead in the NIPT market, holding a significant share driven by favorable reimbursement policies and a high adoption rate. Europe continues to be a strong market due to widespread clinical acceptance and growing public awareness. The Asia Pacific region, particularly countries like China and India, represents a major growth opportunity with increasing healthcare expenditure and a large number of births.

𝗠𝗮𝗿𝗸𝗲𝘁 𝗗𝗿𝗶𝘃𝗲𝗿𝘀 𝗮𝗻𝗱 𝗖𝗵𝗮𝗹𝗹𝗲𝗻𝗴𝗲𝘀

𝗠𝗮𝗿𝗸𝗲𝘁 𝗗𝗿𝗶𝘃𝗲𝗿𝘀 📈:

Rising Maternal Age: The global trend of women having children later in life increases the risk of chromosomal abnormalities, driving the demand for NIPT.

High Accuracy and Safety: NIPT offers superior accuracy for detecting common trisomies compared to traditional screening methods, with the added benefit of being non-invasive and risk-free for the fetus.

Growing Awareness: Increased awareness among expectant parents and healthcare professionals about the benefits and availability of NIPT is boosting its adoption.

Technological Advancements: Continuous improvements in NGS and bioinformatics have led to more accurate, faster, and affordable tests, expanding their use.

𝗠𝗮𝗿𝗸𝗲𝘁 𝗖𝗵𝗮𝗹𝗹𝗲𝗻𝗴𝗲𝘀 📉:

High Cost: Despite technological advancements, the cost of NIPT can still be a barrier for many, especially in developing regions where insurance coverage is limited.

Ethical and Regulatory Concerns: Issues surrounding the use of NIPT for sex selection or the detection of incidental findings raise ethical dilemmas and create regulatory complexities.

Limited Infrastructure: A lack of specialized laboratory infrastructure and bioinformatics expertise in some emerging markets can hinder market expansion.

𝗠𝗮𝗿𝗸𝗲𝘁 𝗧𝗿𝗲𝗻𝗱𝘀

Expanded NIPT Panels: A major trend is the shift from screening only for common trisomies to offering expanded panels that include microdeletions, single-gene disorders, and other genetic conditions.

Decreasing Cost of Sequencing: The cost of NGS continues to fall, making NIPT more accessible and leading to higher adoption rates.

Adoption for Low-Risk Pregnancies: Initially used for high-risk pregnancies, NIPT is increasingly being recommended for all pregnancies, including those considered low-risk.

Artificial Intelligence (AI) in Diagnostics: The integration of AI and machine learning is enhancing the accuracy and speed of interpreting NIPT results, particularly for complex chromosomal anomalies.

𝗙𝘂𝘁𝘂𝗿𝗲 𝗢𝘂𝘁𝗹𝗼𝗼𝗸

The future of the NIPT market is exceptionally promising. We can expect to see wider adoption, driven by declining costs, favourable reimbursement policies, and continued technological innovation. The market will likely become more integrated into routine prenatal care globally. Furthermore, the expansion of NIPT to include a broader range of genetic disorders and the potential for direct-to-consumer services will open up new avenues for growth.

𝗞𝗲𝘆 𝗠𝗮𝗿𝗸𝗲𝘁 𝗦𝘁𝘂𝗱𝘆 𝗣𝗼𝗶𝗻𝘁𝘀

The market is largely dominated by cell-free DNA-based testing, which is expected to hold the highest share throughout the forecast period.

Next-generation sequencing (NGS) is the leading technology, providing the highest accuracy and contributing significantly to market growth.

Trisomy detection, especially for Down syndrome, remains the most prevalent application.

North America and Europe will remain key markets, while the Asia Pacific region will be the fastest-growing.

𝗖𝗼𝗺𝗽𝗲𝘁𝗶𝘁𝗶𝘃𝗲 𝗟𝗮𝗻𝗱𝘀𝗰𝗮𝗽𝗲

The NIPT market is a highly competitive and consolidated space, with several key players vying for market share. These companies are focused on product innovation, strategic collaborations, and expanding their geographic footprint.

𝗕𝘂𝘆 𝘁𝗵𝗶𝘀 𝗣𝗿𝗲𝗺𝗶𝘂𝗺 𝗥𝗲𝘀𝗲𝗮𝗿𝗰𝗵 𝗥𝗲𝗽𝗼𝗿𝘁: https://www.transparencymarketresearch.com/checkout.php?rep_id=374&ltype=S

𝗞𝗲𝘆 𝗣𝗹𝗮𝘆𝗲𝗿𝘀 𝗶𝗻𝗰𝗹𝘂𝗱𝗲:

Berry Genetics
BGI
Laboratory Corporation of America Holdings
Agilent Technologies, Inc.
Illumina, Inc.
F. Hoffmann-La Roche Ltd.
NATERA, INC.
PerkinElmer Inc.
Eurofins SCientific
IGENOMIX
Other Players

𝗥𝗲𝗰𝗲𝗻𝘁 𝗗𝗲𝘃𝗲𝗹𝗼𝗽𝗺𝗲𝗻𝘁𝘀

February 2025: Yourgene Health (a Novacyt group company) launched IONA Care+ in the UK, using its IONA Nx NIPT Workflow for safe and accurate testing, aiming to reduce the need for invasive procedures.

May 2024: Natera, Inc. announced the launch of a new cfDNA-based fetal RhD test, providing a timely solution to a nationwide shortage of Rho(D) immune globulin therapy.

April 2025: VeriSeq, a European diagnostics firm, reduced the average cost per NIPT test by 18% after implementing newer, high-throughput NGS platforms, enabling partnerships with mid-sized clinics.

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