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NEAR PATIENT MOLECULAR SOLUTION MARKET ANALYSIS

Near Patient Molecular Solution Market - Global Industry Insights, Trends, Outlook, and Opportunity Analysis, 2022-2028

  • To Be Published : Dec 2024
  • Code : CMI47
  • Formats :
      Excel and PDF
  • Industry : Medical Devices

Near Patient Molecular Solution Market

Near patient molecular solution, also called point-of-care diagnosis, is a technology that helps diagnose and monitor health at the convenience of the patient. There are various innovations in healthcare such as basic health monitoring smartphone apps, wearable devices, and biosensors, which provide ease to patient in monitoring their health. The motive is to provide patients with easy access to testing solutions, with quick turnaround time and accurate results as opposed to that offered by conventional lab-based tests.

Increasing incidence of diseases such as cardiac disorders and diabetes in developing countries, growing preference for home-based point-of-care devices, advancements in technology, and wide availability of easy to use devices are spurring growth of the near patient molecular solution market. According to the institute for Health Metrics and Evaluation (IHME), the number of deaths due to cardiovascular diseases worldwide increased by 41% between 1990 and 2013, from 12.3 million to 17.3 million deaths. South Asia experienced the largest increase in total deaths, with 1.8 million more deaths in 2013 than in 1990—an alarming increase of 97%.

Due to increasing demand for point-of-care diagnosis, manufacturing companies are focusing on developing technologies that provide quick and accurate results, with small learning curve. However, shortage of skilled staff in using these devices is expected to restrain the growth of near patient molecular solution market to a certain extent.

Near patient molecular solution market taxonomy

On the basis of technology, the near patient molecular solution market is segmented as follows:

PCR based: Idylla is a real-time PCR-based molecular diagnostic system designed in such a way that physicians have fast access to highly reliable clinical molecular diagnostic information. Treatments become more targeted to individual patient through personalized medicine.

Genetic Sequencing based: Platforms are available that enables genetic sequencing and analysis of DNA data at point of care with high accuracy. Rapid DNA analysis is expected to gain traction in the near future.

Hybridization based: Peptide nucleic acid (PNA) molecular beacon probe is used to quantify 16SrRNA of specific populations in RNA extract of environmental samples.

On the basis of application, the global near patient molecular solution market is segmented as infectious diseases testing kits, pregnancy and fertility kits, hematology testing kits, urinalysis testing kits, and glucose monitoring kits. Infectious disease kits are further sub-segmented into tuberculosis, human immunodeficiency virus (HIV), hepatitis, and malaria.

Quick turnaround times of Near Patient Molecular Solutions a boon for Hospitals and Private Clinics

End users of near patient molecular solution or POC devices include hospitals, homecare, research laboratories and diagnostic laboratories. Use of near patient molecular solutions provides fast turnaround times for physicians at outpatient care facilities

North America Prominent Market, Asia High Potential Region

North America is a potential market for molecular diagnostics kits used in the testing of infectious diseases. This is due to technological advancements in molecular diagnostic tools, high prevalence of infectious diseases, high patient awareness, and faster adoption of these devices in the region. The near patient molecular solution market in Asia is projected to witness rapid growth due to rampant research and development activities and growing awareness among the populace about infectious diseases and their diagnostic procedures. Moreover, increase in population and growing disposable income in developing countries such as India and China are expected to boost growth of the near patient molecular solution market in the near future.

Global players involved in near patient molecular solution market

Major companies operating in the global molecular diagnostics include Abbott Laboratories, Becton, Dickinson and Company, Thermo Fisher Scientific Inc., F. Hoffmann-La Roche Ltd, Siemens AG, Veridex, LLC, Luminex Corp., and GenMark Diagnostics. Integration of advanced technologies in their product offerings is the major focus of companies competing in near patient molecular solution market. Abbott’s i-STAT Alinity handheld blood testing platform received CE mark in November 2016. Siemens Healthineers acquired Conworx Technology to flesh out its point-of-care informatics capabilities in November 2016. This highly lucrative market is expected to witness fast growth in the near future, fueled by increasing R&D activities by major players in order to differentiate their offerings.

Key Developments

  1. Key players are focused on different business strategies such as product launches, in order to expand their product portfolio and gain competitive edge in the market. For instance, in May 2019, Siemens Healthineers, a subsidiary of Siemens AG launched Atellica Solution at 23rd IFCC-EFLM European Congress of Clinical Chemistry and Laboratory Medicine held at Barcelona, Spain. Atelllica is designed to address common clinical laboratory challenges.
  2. Major players in the market are involved in various business strategies such as gaining regulatory certification, in order to enhance their market presence. For instance, in June 2019, Becton, Dickinson and Company announced CE-IVDD certification for BD COR System in Europe. This high throughput solution is indicated for disease diagnostics that sets new standards in automation for molecular testing.
  3. Major players in the market are involved in various business strategies such as gaining regulatory certification, in order to enhance their market presence. For instance, in December 2018, Becton, Dickinson and Company received the U.S. Food and Drug Administration 510(k) clearance for its BD MAX enteric viral panel. This is a molecular diagnostic test for direct qualitative detection and differentiation of enteric viral pathogens.

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About Author

Komal Dighe is a Management Consultant with over 8 years of experience in market research and consulting. She excels in managing and delivering high-quality insights and solutions in Health-tech Consulting reports. Her expertise encompasses conducting both primary and secondary research, effectively addressing client requirements, and excelling in market estimation and forecast. Her comprehensive approach ensures that clients receive thorough and accurate analyses, enabling them to make informed decisions and capitalize on market opportunities.

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