Endotoxin testing is majorly used in industries such as medical devices, pharmaceutical, research, and biopharma. It is put to process at various stages of manufacturing and development of bulk lot release testing, raw material testing, and final release testing. These tests are carried out to detect the presence or absence of endotoxins released by non-gram organisms. The presence of endotoxins can lead to severe conditions like septic shock symptoms, fever, and pyrogenic response if they enter the bloodstream of a patient. This makes endotoxin testing a primarily required process in the biomedical and pharmaceutical industries. An increment in the development of biotechnology instruments/systems, medical devices, and pharmaceutical products has increased significantly, leading to increased demand for endotoxin testing. The rising inclination towards outsourcing to contract manufacturing organizations for endotoxin testing and other contamination testing purposes has been rising significantly in recent years. As a result, it is safe to say that several lucrative opportunities float across the global market.

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People and Governments Become Safety-Sensitive, Encouraging Practice of Widespread Endotoxin Testing and Pushing the Market toward Fruition

Increase in health standards and need for disease specific drugs have caused a boom in demand for novel therapeutic medical drugs and devices. Through the manufacturing of such devices and drugs, the demand for endotoxin testing has also grown drastically. Fast-paced adoption of technology within the biopharmaceutical industry owing to increased contamination cases has become a key driver of market growth. Similarly, escalation in public and regulatory concerns about product safety is encouraging the use of endotoxin testing. As an increasing number of countries make their way toward economic development, healthcare needs and quality standards are expected to increase, impelling maturity in product development and researches. Moreover, staggering global demand for research and development investments in the life sciences industry is set to propel market growth in upcoming years.

Developed Regions Lead Global Market Growth, While Developing Countries Rely on Indigenous Market Expansion

Geographically, the market for endotoxin testing is divided into a total of five regions viz. North America, Asia Pacific, Latin America, Europe, and Middle East & Africa. North America has the most number of regulatory guidelines established for the safety and benefits of citizens; this easily makes it the dominating region. The economically-developed countries of Asia Pacific are also expected to undergo rapid increment in the market demand.

Fresh Innovations, Acquisition Strategies, and Technological Advancements Prove Advantageous for Key Market Players

Global demand for endotoxin testing market is forecasted to impel in the near future as industry players bring in newer methods like Endosafe-PTS test by Charles River Laboratories and USP chromogenic method by Sigma-Aldrich. Moreover, industries are enhancing their capacities by acquiring other companies with expertise in endotoxin testing. For instance, in December 2016, Fujifilm acquired Wako Pure Chemical Industries, Ltd. for US$ 1.40 billion. The synergy is expected to help Fujifilm in the field of regenerative medicine, contract development and manufacturing organization, and in-vitro diagnostics.
Other key players in the market include Accugen Labs, Wako Chemicals USA, Inc., Charles River Laboratories, Inc., Pacific BioLabs, Lonza, STERIS, Nelson Laboratories, LLC, Bio-Synthesis Inc and Biogenuix.

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