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Pharmaceutical dosage form testing systems are used to verify the efficacy and bioavailability of a drug formulation. The evaluation and assessment of a tablet’s chemical, physical, and bioavailability properties are especially important in tablet design and for monitoring product quality. Various standards should be used to control the pharmaceutical quality of tablet dosage forms. The standard QC tests carried out on tablets include weight variation, content uniformity, diameter and thickness, hardness, friability, disintegration, and dissolution. It is imperative to test for formulary stability and potential drug degradation. Dosage form testing also verifies the physical strength of formulation. Pharmaceutical dosage form testing systems have additional features such as vibration-free tablet separation, auto separation and auto alignment.

Numerous tests are performed at every stage of production to ensure that quality is not compromised and that Good Manufacturing Practices are followed. Quality checks are crucial to the pharmaceutical industry as they guarantee the patient a safe and effective product and further, protect the manufacturer against compensation claims.

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Pharmaceutical dosage form testing systems ensure that a quality end product reaches the end consumer, which is a key factor anticipated to propel the demand for pharmaceutical dosage form testing systems worldwide.

Market Dynamics:

The global pharmaceutical dosage form testing systems market is expected to register a significant CAGR over the forecast period. Several regulations imposed by various organizations, such as the U.S. FDA, across the globe necessitate quality checks in the manufacturing of pharmaceutical drugs to ensure the quality, efficacy, and safety of capsules and tablets, which in turn is anticipated to boost the demand for pharmaceutical dosage form testing systems. The introduction of advanced technology based dosage form testing systems is also driving the growth of the global pharmaceutical dosage form testing systems market.

However, the high price of pharmaceutical dosage form testing systems may act as a restraint for the global pharmaceutical dosage form testing systems market over the forecast period. Additionally, the dearth of skilled personnel for operating pharmaceutical dosage form testing systems is also creating a hurdle for the growth of the said market.

Regional Outlook

On the basis of regional presence, the global pharmaceutical dosage form testing systems market can be segmented into eight key regions: North America, Latin America, Western Europe, Eastern Europe, Asia-Pacific excluding China and Japan (APCEJ), China, Japan and Middle East & Africa. North America is pegged to dominate the global pharmaceutical dosage form testing systems market with a leading share in terms of revenue. The market in the region is expected to register significant growth over the forecast period, owing to technological advancements and the presence of developed medical infrastructure. Europe, followed by North America, is slated to hold a moderate share and register a healthy growth rate in the global pharmaceutical dosage form testing systems market.

APECJ and China are emerging as lucrative markets for pharmaceutical dosage form testing systems and are anticipated to register significant shares over the forecast period due to the increasing demand for these systems and developing medical infrastructure in the regions. Latin America and MEA are at a nascent stage in the global pharmaceutical dosage form testing systems market and are expected to exhibit moderate growth over the forecast period, owing to the increasing medical facilities in these regions.

Market Participants:

Some of the market players in the global pharmaceutical dosage form testing systems market include SOTAX AG, ABC Laboratories, Almac, Dalton Pharma Services, GEA Process Engineering, Micromeritics Instrument Corporation, Quality Chemical Laboratories and SCYNEXIS, Inc.

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An animal microchip implant is an innovative technology used for tracking pet animals and other healthcare issues in animals. Microchips implanted in pet animals are used to track the movement of pets to prevent the loss of pet animals. A microchip implant is a small device that can be implanted under the pet’s skin and works as an identification for that particular pet with all the pet’s information. Microchips implanted in pets have all the basic details, such as owner’s name and address and vital details with past and present medical history. Microchips have a 15-digit number, which can be scanned under a database for all the major and minor details of a pet. They provide real-time data of a pet’s locations. Two types of microchip implants are available in the market. The first, surgery-injectable implants, need be placed by veterinary surgeons and the second are available as self-implanted injectable microchips. Many tags are also available, which can be placed near the neck or other tag areas on pets. Apart from pet animals, farm animals are also implanted with microchips to monitor the activities of farm animals and track details such as vitals, health-related information and other details pertaining to the farm or the owner.

Animal Microchip Implant Market: Drivers and Restraints

The animal microchip implant market is pegged to witness significant growth over the forecast period as pet adoptions are increasing and pet owners are becoming more aware regarding the technology. Players such as Wuxi Fofia Technology Co., Ltd, and Autag Technology Europe BV are creating a database of all animals, including pets and farm animals. Technological advancement is a major contributor to the increase in the number of animal microchip implants across the globe. On the other hand, lack of focus in veterinary health expenditure, lack of awareness regarding implant use and process to implant inside or outside the animals and others factors are expected to hinder the growth of the market.

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Animal Microchip Implant Market: Overview

The animal microchip implant market is primarily driven by increasing pet adoption and awareness about animals. Animals are well managed with the help of microchip implants, which provide all the necessary details needed by animal owners. This has resulted in an increase in the number of microchip implants in animals. Other factors leading to the growth of the animal microchip implant market include the increasing number of animal management systems in farms and individual animal owners.

Animal Microchip Implant Market: Region-wise Outlook

Geographically, the animal microchip implant market can be segmented into North America, Latin America, Western Europe, Eastern Europe, Asia Pacific, Japan, Middle East and Africa. North America is the major market for animal microchip implants as animal health expenditures in the region are relatively high as compared to other regions. Additionally, pet adoption is increasing among the population and individuals are aware of veterinary health managements with animal monitoring. Europe and Asia Pacific are growing markets for animal microchip implants as microchips help monitor and manage animals and the introduction of new veterinary technology is increasing in these regions. The MEA region is also focusing on animal management and protection.

Animal Microchip Implant Market: Key Players

Some of the players identified in the animal microchip implant market include Zee Tags Ltd, Autag Technology Europe BV, Wuxi Fofia Technology Co., Ltd, I.D.ology, Microchip Identification Systems, Inc., Pet-ID Microchips Ltd, Shenzhen ZDCARD Tech Co., LTD, Quanzhou Hecere Electronic Limited, Ningbo Luke Medical Devices Ltd,  and other Radiofrequency identification (RFID) animal microchip manufacturers.

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Cell block offer the opportunity to examine the histological structure and allows the use of ancillary tests. The automated cell block system from Cellient™ addresses the limitations of traditional cell block methods by providing an automated method for creating cell blocks, filter technology ensures cell capture even in scant cases. Also samples prepared with the automated cell block systems are well-matched with immunohistochemistry, in situ hybridization and routine special stains. Cell block is a process for preparing cytological material with the goal that it can be prepared, segmented, recolored, and seen as a histology segment. It can give analytic and diagnostic data notwithstanding that got from cytology slides. Mechanization likewise constructs reproducibility, and streamlines both assembling and downstream handling. In the following decade, cell-based treatments will turn out to be progressively normal for immunological disorders, cancer, heart failure and other different conditions. Cell-based assay segment of research facility automation presently represents around 25% of computerized systems utilized for fluid mechanics coupled with advanced automation.

Market Dynamics of Automated Cell Block Systems Market

A number of factors drive the growth of the automated cell block systems market. Some of these include the increase in the production capacity for automation systems by enhancing and overcoming the limitations of traditional cell block methods and penetration of new products with higher uniformity, cellularity & transparency. To fulfil the demand, device manufacturers have grown completely mechanized, end-to-end frameworks with an extensive variety of new automation systems with higher technology assessment. Top advantages include, availability of block facilitates more sections, concentrated in a small area of slide so that examination is less time consuming. Loose cells, cell aggregates and microscopic tissue fragments are easily recoverable. Other features include, stains of immunocytochemistry, pattern and architectural recognition of tumor is possible, no necessity of biopsy is required and storage of cell blocks is easier than unstained slides. Most of the research facilities would profit fundamentally from counselling a specialist to help manage the procedure. While picking a framework, numerous research centers that have effectively done the switch found that the most basic variables are usability, institutionalization, and adaptability. Technology assessment in the automated cell block systems with higher turnaround time coupled with faster processes and government initiatives to aid the development of the market is gaining traction. However, high cost of automated cell block systems and complex regulatory framework slightly hinder the growth of the automated cell block systems market.

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Automated Cell Block Systems in Laboratories

With the traditional method of culturing and testing the results could take days and it can be of sub-optimal quality coupled with inconsistent results, insufficient cellularity, long processing times, and risk of contamination may occur. With the automated cell block systems, it helps maintain crisp, clear cellular architecture, minimizes operator error, captures available cells, maximizing cellularity even from small samples, produces standardized and consistent preparations in less than an hour, and also cross reduces contamination risk. There is a need to reduce the time required for the detection process. This can be achieved by the use of automated cell block systems.

Regional Market Outlook

Although North America will continue to hold the largest share in the automated cell block systems market, Asia-Pacific is expected to grow with the largest CAGR.  The continued focus of the major player towards emerging and Asian countries as well as due to the support of the government in these region leads to development of the automated cell block systems market in the region.

Competition Outlook

Key players in the automated cell block system market are: Hologic, Inc., BioTek Instruments Inc., Miltenyi Biotec, Avantor, and others.

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With the millions of Americans being overweight, a large number of canine companions comprising about 20% to 30% of dogs are overweight in the United States. Two main reasons for dogs being overweight are too little exercise and over eating. As per the Veterinary Medical Association, obesity is considered as the fourth leading cause for death among canines. Dogs that falls under category of overweight or obese are prone to various diseases including heart disease, skin and coat problems, arthritis, trouble breathing, and difficulty in controlling their body temperature.

However, other factors such as slow metabolism, neutering, and hormonal disorders including hypothyroidism and Cushing’s disease can cause weight gain in dogs. In response to this predominant problem of obesity in dogs, recently various companies are focused on developing the FDA approved drugs to treat conditions such as obesity in dogs. For instance, Slentrol, the first FDA approved diet drug has been recently developed by Pfizer Animal Health for canine obesity. This diet drug suppresses the dog’s appetite and blocks fat absorption in their bodies. This drug is administered orally directly into dog’s mouth or food. On an average, dogs are expected to lose 3% of their weight every month. However, these weight loss drugs have side effects that includes intermittent vomiting or diarrhoea.

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These pharmaceutical drugs inhibit the transfer of dietary fats from dog’s intestinal cells into the blood stream. The accumulation of these dietary fat in the intestinal cells is supposed to increase release of intestinal hormones that induces signal of fullness in the dog’s brain, reducing his appetite. Canine weight loss drugs are capable of extreme performance and allow significant weight loss in dogs when coupled with proper food diet, thus contribute majorly to the revenue generation in canine weight loss drugs market. Therapeutic diets vary extensively in its ingredients, fiber concentrations and nutritional profiles, so significant therapeutic diet options are available for a comprehensive range of dog patients.

These canine weight loss drugs are broadly used to treat obese conditions in dogs that experience greater demand and are only available via veterinarians or a veterinary prescription, thus generating large revenues in the canine weight loss drugs market. Canine weight loss drugs market on the basis of drug type is classified into Slentrol (Dirlotapide), Orlistat (Xenical), Lorcaserin (Belviq), Naltrexone HCl and bupropion (Contrave), Liraglutide (Saxenda), Phentermine and Phentermine and Topiramate (Qsymia). However, the main distribution channel for canine weight loss drugs include hospital pharmacies, retail pharmacies, drug stores, e-commerce and others.

On the other hand, canine weight loss drugs market is gaining profit due to rising incidence of chronic heart diseases in obese dogs across the globe. As per a clinical survey conducted by Association for Pet Obesity Prevention in 2017, 56% of dogs and approximately 60% of cats were classified as clinically overweight or obese in United States by the veterinary healthcare professionals. The growing incidence of obesity in dogs tend to propel the growth of canine weight loss drugs market across the globe.

Canine weight loss drugs consist of various drugs used for treatment of obesity or overweight conditions in dogs and register a significant revenue growth in the canine weight loss drugs market. The growing adoption of pet weight loss drugs by the veterinarians is further anticipated to drive the demand for canine weight loss drugs and thereby increasing revenue generation in canine weight loss drugs market.

Canine Weight Loss Drugs: Market Dynamics

Growing awareness regarding canine weight loss drugs among veterinarians, availability of cost effective canine weight loss drugs in the market, and high prevalence of obesity in dogs across the globe is expected to be the key factor driving growth of canine weight loss drugs market. Some of the devastating consequences of obesity including trouble breathing, greater risk for heat stroke, diabetes, orthopedic concerns, reduction in life span and others are responsible for increased need to reduce weight in dogs.

Thus, the demand for canine weight loss has registered an upsurge, thereby generating more revenues in canine weight loss drugs market. Also, developed veterinary care infrastructure and rising veterinary care spending are some other factors propelling the growth of canine weight loss drugs market. Also, rise in FDA approvals for canine weight loss drugs and increasing opportunity to help pets manage their weight is further expected to drive the growth of canine weight loss drugs market. However, side effects such as vomiting, diarrhoea, and lethargy, and non-recommendation of these drugs for dogs with liver disease, or receiving corticosteroids, and pregnant or nursing dogs are some of the factors restraining the canine weight loss drugs market growth.

Canine Weight Loss Drugs Market: Key Players

Some of the key players present in global canine weight loss drugs market are Pfizer Animal Health, GlaxoSmithKline plc., Arena Pharmaceuticals, Inc., Takeda Pharmaceuticals U.S.A., Novo Nordisk A/S,  Cigna and others.

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Premature births have become very common. Premature babies also called preemies require extra care than the full-term babies. Premature birth occurs due to infections, stress, chromosomal abnormalities, maternal age, and chromosomal abnormalities. Premature babies have weak immune system and underdeveloped parts that include the skin, lungs and digestive system. Technology advanced devices have been developed, which monitor the heart rate, respiratory rate, blood pressure, and temperature of the premature baby. More efforts are being put up by the manufacturers in order to develop equipment that function efficiently. Also, equipment such as wireless camera system has been developed by the manufacturers, which remains contactless with the premature babies and detects their movement nonstop. It detects even the slight changes in the skin colour, heart beats, and movements of its shoulders. Moreover if the baby does not suffer from any problem and has a normal heart & breathing rate the baby is given Kangaroo care. This is a technique where the baby is held skin to skin contact with the mother for an extended time which provides the baby the apt temperature (warmth if the baby is cold and vice versa), protects from infection, increase weight gain and provides safety and affection. These equipment and techniques can save a lot of pre-mature babies from dying.

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Factors Driving the Growth of Premature Baby Monitoring Equipment Market

The demand for premature baby monitoring equipment has increased due to increasing number of deaths of premature babies. According to GE health care, over 15 million pre-mature babies are born worldwide every year and more than 1 million children die. Rise in the demand for the equipment and cases of premature occurrences are driving the growth of the market. Moreover, enhancement in the healthcare infrastructure is also playing a vital role in the growth of the market. The companies are providing technically advanced and efficient products which provide oxygen, maintain temperature, monitor the heartbeats and protects from cold temperatures.

Increasing birth rate in developing countries such as Asia pacific is driving the demand for premature baby monitoring equipment with the rising awareness. Moreover, the demand for premature baby monitoring equipment is going to rise globally with the rise in the population in countries such as India and China, which account for highest birth rates. Also, increasing prevalence of infections acquired in the hospitals in premature babies is further challenging the growth of the market. However, decreasing birth-rates in developed countries and poor approach towards the premature babies in the developing countries can restrict the growth of the market. Increasing investment and R&D will overcome the deficiencies for better alternatives for the growth for the premature baby monitoring equipment market.

Regional Market Outlook

Geographically, the global premature baby monitoring equipment market is segmented into seven key regions, namely North America, South America, Eastern Europe, Western Europe, and Asia Pacific excluding Japan, Japan and Middle East & Africa. North America followed by Europe is the dominant market of premature baby monitoring equipment due to technological advancement, infrastructure and better health care facilities. On the other hand, Asia pacific is expected to grow during the forecast period due to the rise in the birth rates and increasing government initiatives. The government is creating awareness programs for providing better healthcare facilities for the children by increasing public expenditures. Moreover the manufacturers are investing on the premature baby monitoring equipment due to huge demand by the end users.

Key Participants

Examples of some of the key players in the global premature baby monitoring equipment market are Analogic Corporation, GE Healthcare, Koninklijke Philips N.V.; Medtronic plc; CooperSurgical, Inc.; Stryker, Olympus Corporation, Drägerwerk AG & Co. KGaA,, Novamed USA, Weyer, Fisher & Paykel Healthcare, BabyBloom Healthcare, Novos Medical Systems, etc.

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Future Market Insights (FMI) is a leading provider of market intelligence and consulting services, serving clients in over 150 countries. FMI is headquartered in Dubai, the global financial capital, and has delivery centers in the U.S. and India. FMI’s latest market research reports and industry analysis help businesses navigate challenges and make critical decisions with confidence and clarity amidst breakneck competition. Our customized and syndicated market research reports deliver actionable insights that drive sustainable growth. A team of expert-led analysts at FMI continuously tracks emerging trends and events in a broad range of industries to ensure that our clients prepare for the evolving needs of their consumers.

Contact Us:

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Cranial injuries can create permanent disabilities in the brain and scalp which impacts on a person’s life and his personality. Injuries can be caused due to road accidents, falls or sports related accidents are often lead to severe cranial injuries. These injuries will include skull fractures, scalp wounds, conclusions and many more. These injuries can be closed without breaking or opening the skull which may affect the brain. Fractures in the skull leads to break in the cranial bone. Cranial fixation is a technique for stabilizing a variety of fractures of skull. Non-resorbable cranial fixation systems includes horse shoe headrests Horseshoe Headrests, Skull Clamps and accessories like pins and forceps. The skull clamps provide fixation in prone lateral and sitting positions. After surgery of the patient, cranial fixation systems stabilized the head position in order to prevent movements and any further complications. The horse shoe headrest also provide a support for both infants and adults so that the neck and the head remains positioned. It is used for both vertical and lateral movements while the open area makes the space for chin. The procedure or treatment for repairing the cranial vaults is called Cranioplasty. The usage of non- resorbable cranial fixation systems helps in the healing of the bone and improves the 3-D position. However, the metal like titanium used during the fixations may impact on the images later on during CT- scans and MRI. Hence, the non resorbable cranial fixation systems would witness a healthy adoption among surgeons over conventional metal based fixation systems.

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Factor driving the Non- Resorbable Cranial Fixation System Market

Non- resorbable cranial fixation system market is primarily driven by increasing number of cranial injuries cause due to road accidents and acute brain injuries. According to a report by Centers for disease control (CDC) in 2013, approximately 50,000 people died due to chronic brain injuries in the U.S. Non-resorbable cranial fixation system market in North America region is dominant due to the increasing neurological diseases which required invasive neurosurgical treatment. The uncertainties associated with the use of Non- Resorbable Cranial Fixation System and lack of clarity in insurance coverage and reimbursement are constraining the growth of Non- Resorbable Cranial Fixation System market to a large extent. Moreover the growth of the market is expected due to the powerful regulations and patient safety. Non- Resorbable Cranial Fixation System Market offers the potential to identify the cranial injuries and holds a strong perception in future with its continued investment.

Regional Market Outlook

Geographically, Non- Resorbable cranial fixation system market is segmented into North America, Latin America, Europe, Asia-Pacific, and Middle East & Africa and Japan. North America region is expected to dominate the Non- restorable cranial fixation system market globally followed by Europe. North America is the dominant Non- restorable cranial fixation system market due to the high prevalence of neurological and brain injuries in the region. Non- Resorbable cranial fixation system in Asia Pacific region is expected to grow at a fastest growth rate with the awareness programs and growing number of geriatric population suffering from chronic and end stage neurological disorders which requires surgical intervention. In addition, increasing number of road accidents and other manmade disasters resulting in acute brain injuries. This increase in number of patients with severe brain injuries would increase the demand for cranial fixation system. The increasing demand for cranial fixation system would results in growth and development of the cranial fixation system market in Asia Pacific region. Ready availability of cranial fixation devices and instruments in regions such as Asia Pacific and Latin America is further expected to increase the adoption among hospitals which will spur the revenue growth during the forecast period.

Some of the major players identified in Non- Restorable Cranial Fixation System Market are B. Braun , Changzhou Huida, DePuy Synthes, Medtronic, OsteoMed, Stryker, Evonos, Integra, KLS Martin, Jeil Medical, NEOS Surgery.  The Companies are involved in collaboration agreements in order to exploit maximum potential. Also they are mainly focused to strengthen the core competencies of their product portfolio.

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Contact Us:

Mr. Debashish Roy
Unit No: AU-01-H Gold Tower (AU), Plot No: JLT-PH1-I3A,
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United Arab Emirates
MARKET ACCESS DMCC Initiative
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ALAD Porphyria (Aminolevulinic acid dehydratase porphyria) is a rare disease caused by the deficiency of 5-aminolevulinic acid dehydratase in the body. It results in an increase in ALAD in liver, blood, urine and other tissues. It is also associated with an increase in erythrocyte protoporphyrin and urine coproporphyrin. It is an autosomal recessive disease and it mostly affects only male patients. Treatment mainly includes enzyme inhibitors derived from processed red blood cells and symptomatic therapy. In symptomatic therapy, NSAIDS, anti-emetics and others are used to manage the disease.

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ALAD Porphyria Treatment Market: Drivers and Restraints

FDA’s Office of Orphan Products Development (OOPD) and Orphan Products Clinical Trials Grants Program (formerly known as Orphan Products Grants) supports the clinical development of products to be used for treating rare diseases or conditions where no current therapy exists or where the proposed product will be superior to the existing therapy and this will fuel the growth of the ALAD porphyria treatment market. Along with this, FDA also provides grants for clinical studies on safety and/or effectiveness that will either result in or substantially contribute to market approval of these products. Other factors, such as the fact that the growing demand for orphan drugs is inelastic, meaning that it is relatively insensitive to any changes in prices, will also add to the growth of the ALAD Porphyria treatment market. Orphan drugs are developed for conditions where there are only a few effective treatment options available. A relatively small fraction of the affected population allows the cost of the drug to not severely strain the healthcare system and this will boost the growth of the ALAD porphyria treatment market.  Orphan diseases are supported by well-organized patient-advocacy organizations, including the National Organization for Rare Disorders in the U.S. and EURORDIS in the EU. It may be politically untenable for a payer to refuse coverage for a promising new therapy on cost grounds.

Healthcare providers do not have adequate information regarding the treatment and management of disease. Most people suffering from rare diseases do not have any treatment options available for their condition. Awareness and understanding of rare diseases is often low and many patients struggle to find adequate information about their condition. This particular factor will restrain the growth of the ALAD porphyria treatment market.

ALAD Porphyria Treatment Market: Market Overview

The global ALAD Porphyria Treatment market is witnessing rapid growth due to rising demand for ALAD Porphyria Treatment. There have been a number of initiatives aimed at raising awareness. The Global Genes Project, one of the leading rare and genetic disease patient advocacy organizations in the world, plans to sponsor grassroots activities to increase awareness internationally. The Rare Disease Day is a global initiative aimed at increasing awareness about rare diseases for both healthcare professionals and the population at large. Along with this, many government agencies, educational institutions, clinical centers and corporations have signed on as Rare Disease Day Partners. The future of ALAD Porphyria Treatment market is anticipated to grow with double digit CAGR during the forecast period.

ALAD Porphyria Treatment Market: Region-Wise Overview

The global ALAD Porphyria Treatment Market is segmented into North America, Europe, Asia -Pacific & Japan, Middle East and Africa regions and Latin America. North America dominates the global ALAD Porphyria Treatment Market due to growing high awareness and in North America, the USA is expected to be a major stakeholder due to the high penetration. Economic conditions in the APAC region are set to drive the ALAD Porphyria Treatment market to new heights. European and APAC are expected to be fastest growing regions due to rising awareness about ALAD Porphyria Treatment. Latin America is expected to grow at a stable pace due to increasing acceptance of ALAD Porphyria Treatment. The Middle East and Africa regions are showing significant growth because of growing awareness regarding ALAD Porphyria Treatment. However, developed countries will maintain their position in the ALAD Porphyria Treatment market because of increasing awareness and rising adoption.

ALAD Porphyria Treatment Market: Key Participants

Some of the key participants in the ALAD Porphyria Treatment market include Recordati Rare Diseases Inc., Teva Pharmaceutical Industries Ltd., Novartis AG, Pfizer Inc., Johnson & Johnson, Mylan N.V., AstraZeneca Plc. and others.

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