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Non-Invasive Prenatal Testing (NIPT) Market Key Vendor Landscape By Regional Output, Demand By Countries And Future Growth

 Non-invasive prenatal testing (NIPT) is a sophisticated method used for the screening of chromosomal abnormalities developing in the fetus. Currently, NIPT is considered a valuable test for the pregnant women to provide cost-effective and highly efficient early diagnosis of genetic disorders. Moreover, advancements in genome sequencing technologies reduce turnaround time and the complexity of diagnosis with next generation sequencing (NGS). The NGS technology provides several opportunities to develop the non-invasive diagnostic procedures for an early and accurate detection of various genetic disorders. The life science industry is witnessing significant growth of NIPT tests developed using the NGS technology. Several biotechnology companies are now indulging in the research and development of such NGS-based NIPT products. Furthermore, the advent of genome sequencing technologies in the life science industry has enabled the companies to detect the genetic diseases at an early stage and provide accurate results to remain competitive in the market. 

The NIPT market is currently at a blooming phase, with the presence of various juggernauts such as F. Hoffmann-La Roche Ltd, Illumina, Inc., Agilent Technologies, Inc., BGI, Laboratory Corporation of America Holdings, and PerkinElmer Inc., as well as other medium and small-medium enterprises, that are offering wide range of NIPT products and services in the market. Several companies are attempting to enter the market and sustain themselves in the competition by adopting different strategies varying from partnerships and collaborations to business expansions and product launches.

Market Segmentation

•    By Test – Panorama and Vistara; MaterniT GENOME, MaterniT 21 PLUS, informaSeq, Verifi and Verifi Plus Prenatal Tests; Harmony Test; NIFTY Test and NIFTY Test Pro; QNatal Advanced; PrenaTest, GeneSafe, and PrenatalSAFE; Bambni Test; IONA and Sage; and Others

•    By Platform– PCR, NGS, and Others

•    By Method – cfDNA and FCMB

•    By End User – Hospitals, Clinics, Diagnostic Labs, and Others

•    By Application – Trisomy Detection, Microdeletion Detection, Sex Chromosome Aneuploidy Detection, Others


Regional Segmentation

•    North America – U.S., Canada

•    Europe – Germany, U.K., France, Italy, Switzerland, Spain, The Netherlands, Belgium, Russia, Poland, Denmark, Sweden, and Rest-of-Europe

•    Asia-Pacific – China, Australia, Japan, India, South Korea, Hong Kong, Malaysia, Indonesia, Vietnam, Thailand, Philippines, and Rest-of-Asia-Pacific

•    Latin America

•    Rest-of-the-World


Growth Drivers

•    Increased emphasis on early detection and prevention

•    Availability of advanced screening technologies

•    Increasing consumer demand

•    Shifting of reimbursement policies toward more genetics coverage

•    High incidence rate of Down syndrome

•    Rising average maternal age

•    Increasing prevalence of genetic and congenital disorders


Market Challenges

•    Stringent regulatory guidelines and ethical hurdles

•    Limitations of NIPT

•    Lack of awareness among consumers

•    Alternative screening and testing methods


Market Opportunities

•    Capitalizing on the potential presented by the emerging markets of Asia

•    Availability of direct to consumer tests

•    Focus toward pre-implantation genetic diagnosis


Key Companies Profiled

Agilent Technologies, Inc., BGI, CENTOGENE N.V., Eurofins Scientific, F. Hoffmann-La Roche Ltd., Illumina, Inc., Laboratory Corporation of America Holdings, Natera, Inc., PerkinElmer Inc., Quest Diagnostics Incorporated, Annoroad Gene Technology, MedGenome Inc., Myriad Genetics, Inc., Next Biosciences, and Yourgene Health PLC.

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