| Global Research Trends

Thursday, 18 April 2019

Autoimmune Disease Diagnostics Market Register a Hugh Growth In Healthcare Industry by 2026

The immune system of human body recognize some invaders such as bacteria, viruses, and external chemicals and attacks those to protect the body. However, sometimes the immune system attacks the healthy cells of body by considering them as foreign cells. Such a condition is called autoimmune disease. The autoimmune disease causes abnormal organ growth and changes in organ function. The genes of an individual with environmental exposure might be the major reason for autoimmune disease development. Some of the common autoimmune diseases among over 80 types of autoimmune diseases are type 1 diabetes, systemic lupus erythematosus, inflammatory bowel disease, rheumatoid arthritis. The curing therapy for autoimmune diseases is not yet available only relieving treatments are available for this diseases. Diagnosis of the autoimmune diseases can be done by the tests which involves antinuclear antibody test, antibody test, complete blood counts and some others.

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The growing incidences of autoimmune diseases and government initiatives to boost the autoimmune disease diagnostics market

According to American Autoimmune Related Disease Association (AARDA), in 2016, around 50 million people suffered from autoimmune diseases in the U.S. with 75% being women. Increasing incidence of autoimmune diseases, rising public awareness and government initiatives taken to spend the budget on diagnosis and care services for autoimmune diseases, are some of the factors which are driving the autoimmune disease diagnostics market. Many of the organizations and governments are funding the research and development program for autoimmune diseases, this will help to launch the new products in the market and definitely help in the growth of autoimmune disease diagnostics industry. For instance, the discovery of novel biomarkers, which has proven to be significant to improve the diagnosis of autoimmune diseases is also one of the major factor driving the autoimmune diseases diagnostic market.

The technological advancements in the North America region driving the autoimmune disease diagnostics market

The regional segmentation of autoimmune disease diagnostics market by Coherent Market Insights comprises North America, Europe, Asia Pacific, Africa and rest of the world. North America is of the largest revenue contributor in the global autoimmune disease diagnostics industry. This is mainly attributed to rising incidence of some of the common autoimmune diseases like rheumatoid arthritis and type1 diabetes. The increase in funding by government and private sector, increasing regulatory scenario monitored by World Health Organization (WHO), and technological advancements are some of the factors which are driving growth of the autoimmune disease diagnostics market in the North America region. Asia Pacific is projected to be a fast emerging region in the global autoimmune disease diagnostic market.

The introduction of novel biomarkers in the market will aid in the growth of autoimmune disease diagnostic market

The key players operating the autoimmune disease diagnostics market are Abbott Laboratories, Beckman Coulter, Bio-Rad Laboratories, Euroimmun, Inova Diagnostics, Roche Diagnostics, Siemens Healthcare, A. Menarini Diagnostics, Adaptive Biotechnologies, AESKU Diagnostics, and many others. The government agencies of various countries are increasing their healthcare spending to provide better health care services, and the introduction of novel biomarkers in the research area, owing for ample opportunity for the key players, which in-turn will boost the autoimmune diseases diagnostic market.

Aging population and technological advancements in diagnosis of rheumatoid arthritis will be the cause of growth for rheumatoid arthritis segment

The global autoimmune disease diagnostic market are segmented on the basis of disease type, test type, end user and geography

On the basis of disease type, the autoimmune disease diagnostic market is segmented into:

Systemic Autoimmune Disease diagnostics
Rheumatoid Arthritis
Ankylosing Spondylitis
Systemic Lupus Erythematosus
Some Others
Localized autoimmune disease diagnostics
Multiple Sclerosis
Type 1 diabetes
Hashimoto’s thyroiditis
Idiopathic Thrombocytopenic purpura

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Wednesday, 17 April 2019

Arthroscopy Devices Market Report Puts Limelight On Opportunities By 2025

Arthroscopy is a minimally invasive surgical procedure performed by surgeons to visualize, diagnose and treat the joint related disease. The surgeon makes a small incision through which they insert the probe contain a small lens and lightening system to visualize the inside structure. The arthroscopic surgery is performed to treat the acute or chronic injury related to knee, shoulder, hip and wrist by avoiding post-surgery complications, infection and appears minimum scars at surgery site. There are various applications of arthroscopy devices in knee, shoulder and hip implantation and among these knee implantation contributes the major market share followed by shoulder implantation supported by the increase in cases of knee and shoulder replacement surgery procedures worldwide due to increase in number of obese and aging population.

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Market Dynamics

Rapid advancements in technology has led to increasing adoption of arthroscopy devices, in turn creating a highly conducive environment for growth of the market. It is expected that North America and Asia-Pacific region will show high growth rate during the forecast period, mainly due to increasing geriatric population and growing number of injuries necessitating knee and shoulder surgery. The surgery is especially preferred by sportspersons, due to its low recovery time and minimally-invasive nature. Also, the growth is supported by increased rate of knee surgery. The leading cause behind increased rate of joint pain is overweight and aging population.

High cases of joint replacement surgery is leading the growth of arthroscopy devices market in North America

Increasing incidence of joint replacement in North America is providing opportunity for the growth of arthroscopy devices market. According to Canadian Institute for Health Information (CIHI), around 113,000 knee and hip surgeries are performed in Canada annually. According to the same source, during the period 2009 to 2015, knee replacement surgery and hip replacements surgery increased by 20.3% and 20% respectively. According to Centers for Disease Control and Prevention (CDC), in the U.S. during 2013-2015 nearly 54.4million adults were diagnosed with arthritis and it is expected to reach 78.4million by 2040. These instances will increase the sale of arthroscopy devices in the near future.

The global arthroscopy devices market was valued at US$ 3,910.7 million in 2016 and is expected to witness a robust CAGR of 5.4% during the forecast period (2017 – 2025).

Competitive Landscape

Key companies covered as a part of this study include Smith & Nephew, Olympus Inc., Karl Storz, Stryker Corporation, CONMED Corporation, Vimex Sp. z o.o. and DePuy Synthes Inc.

Detailed Segmentation:

Global Arthroscopy Devices Market, By Product Type:

Arthroscopes
Arthroscopy Shavers
Arthroscopy Fluid Management System
Arthroscopy Implants
Arthroscopy Radio Frequency Systems
Arthroscopy Visualization Systems

Global Arthroscopy Devices Market, By Therapeutic Application:

Knee Implants
Shoulder Implants
Hip Implants
Others

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Electronic Health Record (EHR) Systems Market Register a Hugh Growth In Healthcare Industry by 2026

The systems that are used to maintain digital health record of the patient are called electronic health record (EHR) systems. This systems supports the systematic storage of information such as health progress notes, diagnoses, vital signs, medications, allergies, lab data and past medical history. The electronic storage of the system helps the ecofriendly storage of the information with minimum risk of losing it along with less manual work and other facilities such as easy access to the required information.

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The EHR systems helps to access and track health records conveniently and also allows for easy sharing of patient information with other healthcare professionals, in order to take clinical decisions during the treatment. Furthermore, the system also helps to get connect with different locations and healthcare departments to collect patient data; for instance, from clinical laboratory, other hospitals, in schools for maintaining student’s health record, different companies that keeps the health record of their employees, pharmacies, and emergency facilities. For effective use and to avoid reimbursement loss from any treatment some EHR system providers follow some methods to guide the patient and clinician during the course of treatment.

Technological advancements, highly beneficial applications and raised demand of EHR systems lead the growth for Electronic health record (EHR) systems market towards positive direction in the near future

The continuous improvements in healthcare sector and supportive government initiatives create a highly conducive environment for growth of the global electronic health record (EHR) systems market. For instance, the American Recovery and Reinvestment Act of 2009 authorizes the Centers for Medicare & Medicaid Services (CMS) to provide incentive payments to eligible professionals (EPs) and hospitals who adopt, implement, upgrade, or demonstrate meaningful use of certified electronic health record (EHR) technology. The top contributor region in this market is North America, followed by Europe, as this regions has high adoption rate and developed healthcare network and facilities. The increasing development and digitalization in emerging economies are expected to show the high growth rate in electronic health record (EHR) systems industry in the near future.

Competitive Landscape

Some of the major players in the electronic health record (EHR) systems market are Cerner Corporation, athenahealth, Inc, Meditech, Allscripts, Epic Systems Corporation, Quality Systems Inc, McKesson Corporation and GE Healthcare. Other emerging players in this market are Healthcare Management Systems, eClinicalWorks, Healthland and CureMD Research & Development. Also, the earliest acquisition in this market is Cerner Corporation acquired Siemens Health Services in February 2015. This acquisition will drive the innovation and development in healthcare IT segment.

Electronic health record (EHR) systems market taxonomy:

Global Market by Product Type

Client Server-based EHR Systems
Web/Cloud-based EHR Systems

Global Market by End User

Hospitals
Ambulatory Care Centers

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Peripheral Vascular Devices Market Professional Survey Report 2018-2026

Peripheral vascular disease (PVD), also known as arteriosclerosis obliterans, arterial insufficiency of the legs, claudication, or intermittent claudication, is a blood circulation disorder that causes the blood vessels in the heart or brain to narrow, spasm or block. Peripheral vascular disease usually causes fatigue and pain in the legs and particularly during strenuous physical activities, which usually subsides with rest. The blood vessels supplying oxygenated blood to the arms, kidneys, intestines, and stomach are usually affected by the peripheral vascular devices. According to the Center for Disease Control and Prevention, around 12 to 20 percent of the population in the age category of 60 years and above, developed PAD, in 2016. The incidence rate of this disease is steadily increasing.

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North America held the maximum market share in the global peripheral vascular devices market in 2016. The dominance of this region is attributed to the high adoption of minimally invasive surgeries, high healthcare expenditure as well as patient awareness, among others. Asia Pacific is likely to grow at maximum rate over the forecast period. Presence of a large patient pool with unmet medical need is expected to be a major driver for growth of the market in this region. Improving healthcare scenario in emerging economies such as India and China, among others coupled with the growing GDP of these countries and increasing government initiatives are aiding the growth of the peripheral vascular devices market in this region.

Growing geriatric population to drive the market growth

Growing geriatric population, which is highly susceptible to chronic diseases is expected to create a conducive environment for growth of the peripheral vascular devices market. Additionally, presence of unexploited growth opportunities in the emerging markets such as China, India, and Brazil coupled with rising health awareness among the population are also expected to boost growth of the market in the coming years.

Increasing adoption of bio-absorbable stents coupled with increasing health awareness and growing disposable income among the populace create immense opportunities for the manufacturers in the market. Nonetheless, the high costs of these procedures, particularly in emerging economies and product failures are key challenges faced by vendors.

Top Key Players

Some of the major companies operating in the global peripheral vascular devices market are Abbot Laboratories, Boston Scientific Corporation, Angioscore, Emboline INC, and Bayer AG.

Peripheral vascular devices market taxonomy

On the basis of product type, the global market is segmented into:

Angioplasty Balloons
Embolic Protection Devices
Stents
Inferior Vena Cava Filters
Synthetic Surgical Grafts
Aortic Stent Grafts
Peripheral Vascular Accessory Devices
Vascular Closure Devices
PTA Balloon Catheters
Chronic Total Occlusion (CTO) Devices

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Tuesday, 16 April 2019

Biomedical Refrigerators Market Highlighting Regional Revenue Share Dominance By 2026

Biomedical refrigerators are medical equipment used for storing various biological samples such as biological reagents, medicines, vaccines, blood, blood derivatives, deoxyribonucleic acid (DNA), ribonucleic acid (RNA), and flammable chemicals. Samples with biological origin require accurate conditions for effective storage, which is more effectively provided by biomedical refrigerators in compared with domestic refrigerators. Samples of biological origin are usually available in blood banks, research laboratories, hospitals, educational institutes, and diagnostic centers. Biomedical refrigerators maintain hygiene and consistent temperature in order to reduce the risk of bacterial contamination and explosions of unstable materials, due to which these refrigerators are widely used in blood banks, biomedical laboratories and hospitals. Biomedical refrigerators feature distinct compartments so as to prevent cross contamination and can hold a variety of medical supplies such as blood or vaccines.

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Escalating demand for cellular therapies, blood transfusions, organ transplant, and biopharmaceuticals is stimulating growth of the biomedical refrigerators market. In addition, increasing biomedical R&D activities is boosting demand for biomedical refrigerators, to store biological samples. However, presence of large number of local players and increasing use of renewed equipment are some of the factors hampering growth of the global biomedical refrigerators market. Rampant advancements in technology and infrastructural upgrade of clinics, hospitals, and research laboratories, is expected to fuel growth of the global biomedical refrigerators market over the forecast period.

Factors such as increasing importance on energy-efficient refrigerators are driving the prospects for growth of the biomedical refrigerators market. A major challenge faced by the market includes reduction in energy consumption. According to the current standards, refrigerants are required to have minimum global warming potential, an ozone depleting potential of zero, and be nontoxic as well as inflammable. It is highly challenging to adhere to these standards while maintaining a stable temperature control. Therefore, manufacturers are focusing on developing technologies to maximize efficiency and temperature consistency, while minimizing heat and energy consumption. Improvement of healthcare infrastructure due to the increasing support from government and industry participants to provide technical and financial assistance in procurement of biomedical refrigerators is a positive trend witnessed in the market. These factors in turn, are expected to boost growth of the market in the near future.

North America holds the maximum market share, majorly attributed to presence of high quality standards and high expenses on hospital and healthcare infrastructure in the region. The U.S. spends major share of its GDP toward healthcare, with an aim to improve patient care, reduce the wastage of pharmaceutical and biological components. Growing prevalence of chronic diseases coupled with increasing geriatric population, is triggering research and development that requires appropriate biomedical storage of samples. This is significantly driving the number of blood transfusion procedures, consumption of various pharmaceutical products. This in turn, is boosting demand for biomedical refrigerators across all the end-use segments. Emerging economies such as India, China, and Indonesia are increasingly boosting the expenditure on healthcare infrastructure and medical services.

Major Key Players

Key players operating in the global biomedical refrigerators market include Thermo Fisher Scientific, Aegis Scientific, Inc., Panasonic Healthcare Co. Ltd., Eppendorf AG, Terumo Corporation, Haier Biomedical, Philipp Kirsch GmbH, Leibherr Group, Inc., and Helmer Scientific.

Biomedical Refrigerators Market

On the basis of product type, the biomedical refrigerator market:

Blood Bank Refrigerators
Laboratory Refrigerators

On the basis of end user, the biomedical refrigerator market:

Hospitals
Pharmacies
Diagnostic Centers
Research Laboratories
Blood Banks

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Single-Use Medical Device Reprocessing Market to Witness an Outstanding Growth During 2018-2026

Single-use medical device reprocessing is the concept of sterilizing, repackaging, testing, and manufacturing a used product. There is no clear definition for the term single-use device and it is entirely based upon the end user perception. Reprocessing of single-use device is acceptable, if the device is properly sterilized while keeping its physical and technological functionalities intact. Single-use medical device reprocessing is done in two ways: third party processing and in-hospital processing. Third party processing is considered to be a better option, as regulatory authorities are able to impose strict regulations for validation and quality assurance purpose.

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Single-use medical device reprocessing is gaining popularity as it helps to reduce hospital waste and allows for major cost savings. For instance, Kaiser Permanente, which is an integrated delivery network based in U.S., saved US$ 11 million on an annual basis by reprocessing of single-use devices. Reprocessing enables the hospitals to purchase the same device at a lower price in comparison to the cost of original equipment, which eventually leads to cost savings. Practice Green Health, an NGO providing environmental solutions to the healthcare sector, quoted that single-use medical device reprocessing prevented the entry of 10,000 tons of medical waste during 1997–2007, by processing an estimated 50 million devices. Single-use medical device reprocessing market is poised to grow significantly, as hospitals realize potential cost savings and its ability to reduce environmental hazards.

Cost constraints for Hospitals and positive environmental impact will drive growth of the single-use medical device reprocessing market

Hospitals across the globe are facing cost pressures due to rise in price of original medical equipment. In the U.S., Obamacare and its associated guidelines might get repealed with the change in government. This could lead to low third-party reimbursement for hospitals, in turn influencing them to adopt cost saving initiatives such as single-use medical device reprocessing. The biggest advantage is that hospitals can reduce the cost associated with medical device to 50%, which becomes a crucial factor when dealing with expensive devices such as catheter and cardiac ablation devices. At present, 250 medical devices are already being processed with 10% of medical devices eligible for single-use medical device reprocessing. In terms of environmental protection, hospitals are able to reduce the medical waste to an estimated 50% by the use of single-use medical device reprocessing. Medical waste treatment not only puts enormous cost pressure on hospitals, but in countries such as U.S., China and Japan, it has become a full-fledged industry.

North America is estimated to be the growth pocket for single-use medical device reprocessing market

U.S. has the biggest healthcare system in the world with government spending an estimated 30% of annual budget on healthcare. U.S. is also home to large-sized hospitals such as Cleveland Clinic, Mount Sinai Hospital, Beth Israel Deaconess Medical Centre and Johns Hopkins Hospital. These hospitals are subject to meeting sustainability goals and contain costs at the back of recession. For instance, in 2007, 45% of U.S. hospitals entered into an agreement with third-party processing companies and this number increased to 70% in 2008 due to severe economic crisis. Single-use medical device reprocessing is subject to FDA and required third-party processing companies to maintain quality standards in accordance with the original equipment. FDA formulated stringent regulation to create standardization and avoid infections related to the reuse of single-use devices. FDA has set up a grievance mechanism for reporting of adverse events related to use of single-use device which in turn reinforces accountability.

Single-use medical device reprocessing market is in nascent stage with few players dominating the market

The key players in the single-use medical device reprocessing market are Stryker Corporation, Medline ReNewal, Centurion Medical Products Corporation, Midwest Reprocessing Center, SterilMed Inc., Vanguard AG and Hygia Health Services Inc, among others. These players have successfully demonstrated the impact of single-use medical device reprocessing on cost savings and environmental protection. These companies will benefit in a large manner as the regulatory scenario becomes established in Europe and Asia Pacific.

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Pyrogen Testing Market Necessity And Demand 2018 to 2026

Pyrogen testing is detection of pyrogen in pharmaceutical drugs and devices. The contaminated devices or drugs when introduced in body can cause fever, shock, inflammation, and other problems. Pyrogen testing consists of kits, reagents, and instruments, which enables pyrogen and endotoxins detection by in-vitro methods and minimizes the usage of animal testing.

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Market Dynamics

Increasing research and development in the field of pyrogen testing and advancements in technology for detection of endotoxin is a major factor driving pyrogen testing market growth. According to the Pharma R&D Annual Review, 2018, an estimated drug count in 2017 was around 14,872, while in 2018 it was around 15,267, resulting in an overall pipeline growth by 2.7% in 2018. Stringent government regulations and rising focus on in-vitro testing for detection of pyrogen is one of the major factors boosting growth of the market. For instance, in June 2012, the U.S. Food and Drug Administration (FDA) provided guidelines for pyrogen and endotoxin testing to industries.

The global pyrogen testing market size was valued at US$ US$ 689.9 million in 2017, and is expected to exhibit a CAGR of 12.4% over the forecast period (2018 – 2026).

Increasing demand for testing of pyrogen contamination in medical devices and drugs is expected to propel growth of the pyrogen testing market

Pyrogen testing is used in detection of pyrogen contamination in pharmaceutical dosage forms and medical devices. Pyrogen contaminated injections post administration can cause temperature dysregulation (fever), bodyache, inflammation, shock, multiorgan failure, and other life threatening problems.

Moreover, increasing research and development of therapeutic drugs and medical devices is propelling growth of the pyrogen testing market over the forecast period. According to the United Nations Educational, Scientific and Cultural Organization (UNESCO), November 2016, an estimated US$ 1.7 trillion of global spending in research and development for various medical applications. Moreover, the U.S. Food and Drug Administration (FDA) and its Center for Drug Evaluation and Research (CDER), has approved around 59 novel drugs in 2018 compared to 46 approvals of new molecule entities in 2017.

Key Players

Major players operating in the global pyrogen testing market include Thermo Fisher Scientific, Merck KGaA, Lonza Group, Associates of Cape Cod Inc., Charles River Laboratories Inc., GenScript, WuXi PharmaTech (Cayman), Inc., bioMérieux, Wako Chemicals USA, Inc., Sanquin, Ellab A/S, and Pyrostar

Detailed Segmentation:

Global Pyrogen Testing Market, By Test Type:

Limulus Amoebocyte Lysate (LAL) Test
TAL Test
Monocyte Activation Test (MAT)
Rabbit Pyrogen Test (RPT)
Recombinant Factor C Assay (rFC)

Global Pyrogen Testing Market, By Product Type:

Instruments
Kits
Reagents

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Monday, 15 April 2019

Protein Expression Systems Market - Size, Share, Outlook, and Analysis, 2018-2026

The demand for protein therapeutics has increased considerably, owing to increase in prevalence of chronic diseases and development of plasma-derived therapies. In recent years, proteins expression systems have gained significant traction for therapeutic applications and the number of proteins launched or approved into clinical trials has continually increased. According to the National Center for Biotechnology Information (NCBI) data of 2017, the U.S. Food and Drug Administration (FDA) approved more than 140 recombinant therapeutic proteins for human use and several hundred are currently in development.

However, high cost associated with therapeutic proteins and stringent government regulations towards approval of protein therapies are expected to hinder market growth. For instance, in India, a vial of Avastin (Bevacizumab mostly produced by the mammalian cell expression system), a monoclonal antibody, cost between US$ 372.65 to US$ 402.46. Moreover, immunogenicity is also a major concern for all recombinant drugs, as all biotechnologically produced therapeutics may exhibit some form of immunogenicity.

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Currently, most of all recombinant therapeutic proteins are produced in mammalian cells, mammalian cells are capable of producing high-quality proteins similar to the naturally occurring ones. Furthermore, many approved recombinant therapeutic proteins are generated in E. coli. (Bacteria) due to its well-characterized genetics, rapid growth, and high-yield production.

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Pharmaceutical companies are progressively focusing on research using proteins to develop novel effective therapeutics. Advances in molecular control of gene expression are also expanding the opportunities for protein expression systems. The next generation expression systems are gaining traction as drug manufacturers are looking for cheaper ways to express new biologic drugs. For instance, on 6 December 2018, AMSBIO introduced ALiCE, a new high-yield cell-free protein expression system. ALiCE is a unique eukaryotic system, which yields an unprecedented 3 mg/ml of protein in batch mode.

The production of proteins in appropriate quantity and quality is an essential requirement of the biopharmaceutical and biotechnology industry. Therapeutic proteins provide important therapies for a variety of diseases such as anemia, diabetes, cancer, infectious diseases, and hemophilia. There is a growing demand for recombinant proteins for therapeutic applications. Common therapeutic proteins include antibodies, anticoagulants, hormones, FC fusion proteins, interleukins, and enzymes. Human proteins obtained through genetic engineering play a crucial role in therapeutic medicines.

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Key players operating in the global protein expression systems market include Agilent Technologies, Inc., Becton, Dickinson & Company, Lonza Group Ltd., GenScript Biotech Corporation, Bio-Rad Laboratories, Inc., Merck KGaA, QIAGEN N.V., Thermo Fisher Scientific Inc., Takara Bio Inc., Synthetic Genomics Inc., Lucigen Corporation, Promega Corporation, ARTES Biotechnology GmbH, ProteoGenix, Addgene Inc., Geneva Biotech, Profacgen, and Peak Proteins Ltd.

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Cystic Fibrosis Market with In-depth Insight and Trends Forecast to 2026

Cystic fibrosis (CF) is a genetic disorder that usually affects the lungs and may also affect the pancreas, kidneys, liver, and intestine. Long-term repercussions including difficulty in breathing and coughing as a result of recurrent lung infections can be seen in CF. Some of the other signs and symptoms include sinus infections, poor growth, infertility in males, fatty stool, and guild of the fingers and toes. Different individuals may have diverse degrees of symptoms. CF is chiefly inherited as an autosomal recessive gene. It is triggered by mutations in both the copies of the gene for CFTR or cystic fibrosis transmembrane conductance regulator protein. Individuals with a single copy are carriers. Cystic fibrosis transmembrane conductance regulator protein is involved in the production of digestive fluids, mucus, and sweat. When the protein is not functional, secretions otherwise thin become thick. The ailment is mostly diagnosed by genetic testing and sweat test.

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Over the last few years, advancements in technology have resulted in a shift in research and development towards treatments that target the fundamental cause of the disease by targeting the CFTR function. Moreover, there is an affinity towards licensing the products, and for that reason alliances are being made by a number of biotechnology and pharmaceutical manufacturers, since the majority of the treatments for cystic fibrosis are developed by smaller manufacturers. The increase in licensing activity along with the rise in the number of new partnerships will encourage the smaller companies to continue their research work thereby giving a positive momentum to the cystic fibrosis market.

In spite of significant advancement in cystic fibrosis therapeutics, individuals suffering from CF face significant unmet needs owing to the deficiency of restorative therapies, inadequate choice of mucolytic treatments, and the unvarying fight alongside severe lung infection that needs the expansion of novel antibiotics. These factors are likely to drive the growth of the cystic fibrosis market during the forecast period.

High prevalence of genetic diseases including CF will drive the overall cystic fibrosis market

According to Netwellness, a community service provider, 3 to 4% of the babies are born with genetic disorders. This number is poised to rise in the coming years, especially in the emerging economies of Asia pacific such as China and India owing to high birth rate observed in these regions. As the number of cases of CF rises, so will the demand for CF treatment, thereby augmenting the growth of the overall cystic fibrosis market during the forecast period.

On the basis of geography North America held the maximum market share in the cystic fibrosis market globally. Constructive and favorable regulations and policies as well as high availability of sophisticated healthcare facilities and rising approvals of drugs for treating CF are likely to propel the growth of the cystic fibrosis industry in this region.

Competitor Landscape

Some of the key players operating in the global cystic fibrosis market are AbbVie, Inc., Aradigm, Aurora Biosciences, Bayer AG, Demegen, EryDel, Genentech, Inc., InDex Pharmaceuticals, ManRos Therapeutics, Novartis AG, Polydex Pharmaceuticals, and F. Hoffmann-La Roche AG.

Cystic fibrosis market Taxonomy -

On the basis of therapy type, the global market is classified into:

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Modulators
Protein Transcription Modulators
Pancreatic Enzyme Products (PEP)
Other therapies

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Candidiasis Market Deep Analysis by Production Overview and Insights 2026

Candidiasis is a type of infection caused due to candida—an yeast and also classified as fungus, which is present in the human body. It is usually present in places like mouth, belly, and on the skin. The overgrowth of these leads to an infection. This dormant yeast can lead to candida infection at any stage in a person’s life and is closely linked to the immunity level of the person. There are various types of infections caused due to candidiasis, such as thrush/ oropharyngeal candidiasis, genital yeast infection/ invasive infection, and cutaneous candidiasis. Thrush/ oropharyngeal candidiasis affects the mouth or throat; genital yeast infection affects the vagina; and cutaneous candidiasis is the infection of the skin. When the infection enters into the blood stream, the condition is called Candidemia. Candidiasis can be diagnosed by physical observation. These conditions are usually treated using over-the-counter antifungal medicines and also specific prescription-based antifungal medicines.

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Increasing consumer awareness about candidiasis and growing number of treatment options are major factors fueling growth of the candidiasis market. Conversely, dearth of R&D activities, low product availability, and easy access to alternative treatment methods such as use of herbal medicines inhibits growth of the candidiasis market.

Rising awareness regarding the infection and increasing patient pool to favor the growth of Candidiasis market

Rising awareness about the infections is expected to cause the growth of candidiasis market. Increasing focus of various governments in the APAC region, such as in highly populous China and India, on improving the healthcare infrastructure, along with increasing consumer awareness about the condition is expected to position the region on a high growth trajectory in the global candidiasis industry over the forecast period (2016–2024). Candidiasis are treated using various treatment option such as oral medication, injection, and ointments. Candidiasis can infect males, females and also newborn babies. The condition is notoriously hard to treat in people suffering from diabetes, cancer, AIDS, and also pregnant women. As per stats released by Centers for Disease Control and Prevention (CDC), around 75% of would suffer from at least one vaginal candida infection in their whole life, while 40-45% would suffer twice or more.

Developed Regions Growth Engine of Candidiasis Market

In developed countries, increasing number of organ transplantation, use of catheters, artificial valves, and joints causing to growth of candida infection. The North America and Europe regions account for the largest market share, due to high awareness about the infection, wide availability of treatment and easy access to OTC antifungal drugs creates a highly conducive environment for growth of the market. Azole Drugs holds large market share, with products such as Vfend, Noxafil, and Diflucan being highly preferred among the masses.

Major Key Players

The major market players in Candidiasis market are Bayer, Teva Pharmaceuticals, Stellar Pharma, Pfizer, Wockhardt, Glenmark Pharmaceuticals, Ranbaxy, Taro Pharmaceuticals, and Bristol Laboratories, among others.

Candidiasis Market Taxonomy:

This market is segmented by as follows-

By Route of Administration:

Oral
Parenteral
Topical

By Type of Infection:

Thrush/ oropharyngeal candidiasis
Genital Yeast Infection/ Invasive infection
Cutaneous Candidiasis

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