#Bioburden Testing Market share

[sabalevaishali]

Global Bioburden Testing Market is anticipated to witness value over USD 1.3 billion during the forecast period 2020 to 2027 with a CAGR of over 11%.

Bioburden testing is the study of the microbial count present on the surface of any material or product. The term is used for testing the contamination in pharmaceutical products, food and beverages, medical devices, etc. Bioburden testing is mandatory as per ICH (International Conference on Harmonization) guidelines for the manufacturing and distribution of food and drugs along with medical devices.

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Bioburden Testing Market Registering At Expanding At A CAGR Of 13.7% For Forecast Period From 2019 To 2026: Grand View Research Inc.

San Francisco, 11 March 2020: The Report Bioburden Testing Market Size, Share & Trends Analysis Report By Product, By Test Type (Aerobic Count, Anaerobic Count), By Application (Raw Material Testing, Medical Device Testing), By End Use, And Segment Forecasts, 2019 – 2026

The global bioburden testing market size is expected to reach USD 2.01 billion by 2026, expanding at a CAGR of 13.7% during…

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“Bioburden Testing Market ”report focuses on the market status, future forecast, growth opportunities, market trends and leading players.

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Bioburden Testing Market Strategic Insights and key Business Influencing Factors | Major Players – ., Merck KGaA, SGS S.A., BD., Merck & Co., Inc., North American Science Associates Inc.

Bioburden Testing  Market is the measurement method on medical devices, raw materials or packages of feasible microorganisms. The method enables to determine parameters to guarantee the safety and efficiency of medical devices. It further assists in the regular surveillance of raw materials, parts and installation procedures in the manufacturing system. Bioburden screening is used for the evaluation of drying procedures and the packaging of products is carried out to guarantee safety.

Europe bioburden testing market is registering a substantial CAGR in the forecast period of 2019-2026. The report contains data from the base year of 2018 and the historic year of 2017. The rise in the market can be attributed due increasing using of bioburden screening for quality control in medical, biotechnological and pharmaceutical goods and increasing concern among people about bioburden screening due to microbial contamination.

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Competitive Analysis: Europe  Bioburden Testing   Market

Few of the major market competitors currently working in the Europe bioburden testing market are Charles River, Pacific Bio labs, Inc., Merck KGaA, SGS S.A., BD., Merck & Co., Inc., North American Science Associates Inc., Nelson Laboratories, LLC, Dynatec Labs, Applied Technical Services, Thermo Fisher Scientific, bioMérieux SA,  among others.

Key Pointers Covered in the Europe  Bioburden Testing Market Trends and Forecast to 2026

Europe  Bioburden Testing Market New Sales Volumes

Europe  Bioburden Testing Market Replacement Sales Volumes

Europe  Bioburden Testing Market Installed Base

Europe  Bioburden Testing Market By Brands

Europe  Bioburden Testing Market Size

Europe  Bioburden Testing Market Procedure Volumes

Europe  Bioburden Testing Market Product Price Analysis

Europe  Bioburden Testing Market Healthcare Outcomes

Europe  Bioburden Testing Market Cost of Care Analysis

Europe  Bioburden Testing Market Regulatory Framework and Changes

Europe  Bioburden Testing Market Prices and Reimbursement Analysis

Europe  Bioburden Testing Market Shares in Different Regions

Recent Developments for Europe  Bioburden Testing Market Competitors

Europe  Bioburden Testing Market Upcoming Applications

Europe  Bioburden Testing Market Innovators Study

Get Detailed TOC:

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Scope of the Bioburden Testing   Market

Europe Bioburden Testing Market By Product ( Consumables, Instruments), Test Type ( Aerobic Count Testing, Anaerobic Count Testing, Fungi/Mold Count Testing, Spore Count Testing), Application ( Raw Material Testing, Medical Device Testing, In-Process Material Testing, Sterilization Validation Testing, Equipment Cleaning Validation), End User ( Pharmaceutical & Biotechnology Companies, Medical Device Manufacturers, Contract Manufacturing Organizations, Manufacturers of Food & Beverage and Agricultural Products, Microbial Testing Laboratories), country (Germany, France, United Kingdom, Italy, Spain, Russia, Turkey, Belgium, Netherlands, Switzerland, Rest of Europe)  - Industry Trends and Forecast to 2026

Europe bioburden testing market is registering a substantial CAGR in the forecast period of 2019-2026. The report contains data from the base year of 2018 and the historic year of 2017. The rise in the market can be attributed due increasing using of bioburden screening for quality control in medical, biotechnological and pharmaceutical goods and increasing concern among people about bioburden screening due to microbial contamination.

Bioburden testing is the measurement method on medical devices, raw materials or packages of feasible microorganisms. The method enables to determine parameters to guarantee the safety and efficiency of medical devices. It further assists in the regular surveillance of raw materials, parts and installation procedures in the manufacturing system. Bioburden screening is used for the evaluation of drying procedures and the packaging of products is carried out to guarantee safety.

Market Segmentation: Europe  Bioburden Testing  Market

Europe  Bioburden Testing  Market growing recognition of the medicinal capacity of stem cells in efficient disease management contributes to the development of the industry.

In October 2018, SGS SA has purchased INTER-BASIC RESOURCES, INC. (IBR), a non-clinical contract research organization (CRO). IBR Inc. is a specialist in state-of - the-art experimentation and biopharma technologies for the building of biologics, biosimilar and antibodies and provides multiple screen monitoring and electron tracking facilities. With this purchase, SGS SA would develop its filtration facilities and grow its client profile and client facilities.

In June 2018, QIAGEN announced the introduction of the QIAseq 16S / ITS Panels and the UCP Multiplex PCR Kit with a fresh class of reagents to allow the most precise microbial community profiling of complicated microbiome samples. The fresh QIAGEN devices prevent internal bias in PCR and NGS library preparing with inhibitor-resistant PCR and small bioburden reagents screened for bacterial and fungal DNA contamination.

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The segment that is expected to dominate the market as well as the segment which holds highest CAGR in the forecast period.

Regions/Countries that are expected to witness the fastest growth rates during the forecast period.

The latest developments, market shares, and strategies that are employed by the major market players.

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Key insights in the report:

Complete and distinct analysis of the market drivers and restraints

Key Market players involved in this industry

Detailed analysis of the Market Segmentation

Competitive analysis of the key players involved

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Bioburden Testing Market Similar Report Here:

Biomedical Materials Market

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[morerushikesh]

The Bioburden Testing Market is expected to witness sustained growth over the forecast period (2019-2023).The growth of the Bioburden Testing market is driven as there is favourable growth in the industry is a major factor which will boost the global Bioburden Testing market.

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The Bioburden Testing Instrument market was valued at Million US$ in 2018 and is projected to reach Million US$ by 2023, at a CAGR of during the forecast period. In this study, 2018 has been considered as the base year and 2019 to 2023 as the forecast period to estimate the market size for Bioburden Testing Instrument.

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Pharmaceutical Filtration Market Report 2022 to 2030 By Top Key Players, Types & Applications

The global Pharmaceutical Filtration market is projected to reach USD 25.12 Billion by 2030 from USD 10.9 billion in 2022, at a CAGR of 17.0%.

Pharmaceutical filtration is a separation procedure in which processed materials are passed through a filtration membrane in order to extract undesirable particles from them. This filtration technique aids in removing suspended particles from a medium or solution. It provides considerable and broad sterile and nonsterile filtration of goods for the pharmaceutical production sector. Additionally, pollutants like particle matter and bacteria are eliminated from solids, air, liquids, and gases using filters. The processing of final products, water purification, raw material filtration, cell separation, and air purification are a few other fields where pharmaceutical filtration techniques are commonly used.

Pharmaceutical filtration is a separation method that isolates undesirable components from processed materials by allowing them to pass through a filtration membrane. This filtration technique helps to remove unwanted components from a solution. The single perforated layer, which is frequently employed in applications including raw material filtration, cell separation, final product processing, air purification, and water purification, is used in pharmaceutical filtration.

Segmental Analysis of Global Pharmaceutical Filtration Market:

Based on Product

Systems

Filters

Based on Filters

MEMBRANE FILTERS

Polyvinylchloride

Polycarbonate Tracked Etched

Polyethersulfone

Nylon

Polyvinylidene Difluoride

Polyetrafluroroethylene

Mixed Cellulose Ester and Cellulose Acetate

DEPTH FILTERS

Activated Carbon

Diatomaceous Earth

Perlite

Cellulose

The pharmaceutical filtration market is segmented into three segments- systems, filters and other products. The filter market is further segmented into membrane filters, depth filters, and other filters, such as pre-filters, bag filters, and magnetic filters.

Based on Systems

Reusable

Single Use

In 2021 the filters segment accounted for the largest share of the pharmaceutical market. The large share of this segment is because of the wide use of different types of membrane filters and depth filters for various filtration applications

Based on Filtration Products

Filtration Accessories

Filtration Assemblies

Filter Holders

Based on Technique

Nano-Filtration

Ultra-Filtration

Micro-Filtration

Based on Type

Non-Sterile Filtration

Sterile Filtration

Based on Application

FINAL PROCESSING

Active Pharmaceutical Ingredient Filtration

Viral Clearance

Protein Purification

Formulation and Filling Solutions

Protein Purification

RAW MATERIAL FILTRATION

Bioburden Testing

Media Buffer Filtration

Pre-filtration

CELL SEPARATION

WATER PURIFICATION

AIR PURIFICATION

Based on Scale of Operation

R&D Scale

Manufacturing Scale

Pilot Scale

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Top Key Players:-

Eaton Corporation plc

Sartorius AG

Porvair plc

Amazon Filters Ltd.

Merck KGaA

GE Healthcare

Saint-Gobain Performance Plastics

Kasag Swiss AG

Filtrox AG

Cantel Medical.

Freudenberg Filtration Technologies

Pall Corporation

MMS AG

ErtelAlsop

Danaher Corporation

Meissner Filtration Products

Donaldson Company, Inc

Parker-Hannifin

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Biologics Safety Testing Market Size Analysis, DROT, PEST, Porter’s, Region & Country Forecast Till 2027

The global biologics safety testing market valued of USD 2.79 billion in the year 2017 and is expected to register a CAGR of 13.6% during the forecast period. Biologics safety testing is required for all biopharmaceutical products and vaccines to ensure the product is safe and free of contaminants.

Growing pharmaceutical and biotech industry and increasing demand for biological products are expected to drive the growth of the market. However, stringent government regulations for the approval of biosimilars and high cost of drug development are likely to hamper the market growth over the forecast period.

Regional Analysis:

Geographically, the Americas is expected to dominate the global market owing to the presence of well-established players and rising demand for biological products. Europe is expected to hold the second largest position in the global market owing to the growing pharma and biotech industry. Asia-Pacific is expected to be the fastest growing market owing to the increasing demand for biologics products. Furthermore, the Middle East and Africa region is expected to account for the least market share in the global market.

Segmentation:

The global biologics safety testing market has been segmented into product, test type, and application.

Based on product, the market is segmented into kits & reagents, services, and instruments. The kits & reagents segment is expected to account for the largest share segment of the global market in 2017.

Based on test type, the market is segmented into sterility tests, endotoxin tests, cell line authentication and characterization tests, residual host contamination detection tests, adventitious agent detection tests, bioburden tests, and others.

Based on application, market segmented into vaccine and therapeutics development, blood and blood-related products testing, cellular and safety of biologics therapy, tissue and tissue-related products testing, and stem cell research.

Key Players:

Some of the prominent players in the global biologics safety testing market are Merck KGaA, Charles River Laboratories, Sartorius AG, Lonza Group Ltd., SGS S.A., Thermo Fisher Scientific Inc, Wuxi Apptec, Cytovance Biologics, Inc., Avance Biosciences Inc., and Eurofins Scientific.

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[sabalevaishali]

Bioburden Testing Market is estimated to value over USD 1.3 billion by 2026 end and register a CAGR of over 11% during the forecast period 2019 to 2026.

[healthcareresearchboom]

Biologics Safety Testing Market – Size, Value, Share, Research and Analysis 2026

The global biologics safety testing market is projected to reach USD 6.2 billion by 2026 from USD 3.4 billion in 2021, at a CAGR of 12.4% during the forecast period. The growth of the global biologics safety testing market is driven by factors such as the growth in the biologics and biosimilars markets, growing concerns over cell culture contamination, and rising biopharmaceuticals R&D activities and investments. In addition, emerging markets and increasing biopharmaceutical outsourcing are expected to provide significant growth opportunities for players in the Biologics safety testing market.

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The residual host-cell proteins and DNA detection tests segment accounted for the largest share of the Biologics Safety Testing market in 2020.

Based on test type, the biologics safety testing market is segmented into residual host-cell proteins and DNA detection tests, endotoxin tests, sterility tests, mycoplasma tests, bioburden tests, and virus safety tests. In 2020, the residual host-cell proteins and DNA detection tests segment accounted for the largest market share. The rising demand for residual HCP and DNA detection tests for recombinant proteins and increasing focus on the quality of drugs are the major factors driving the growth of this segment.

The monoclonal antibodies manufacturing segment accounted for the largest market share of the Biologics safety testing market in 2020.

Based on application, the biologics safety testing market is segmented into monoclonal antibodies manufacturing, vaccines manufacturing, blood and blood products manufacturing, cellular and gene therapy products manufacturing, and other applications. In 2020, the monoclonal antibodies manufacturing segment accounted for the largest market share. The large share of this segment can be attributed to the rising prevalence of diseases and increasing government initiatives for the development of monoclonal antibody drugs.

The Asia Pacific region is the fastest growing region of the Biologics safety testing market in 2020.

The Asia Pacific market is projected to witness the highest growth rate during the forecast period, primarily due to the expansion of key market players in emerging Asia Pacific countries, increasing expenditure on life science research, and the increasing trend of pharmaceutical outsourcing to Asia Pacific countries.

Prominent players in the biologics safety testing market are Charles River Laboratories, Inc. (US), Lonza (Switzerland), Thermo Fisher Scientific, Inc. (US), Merck KGaA (Germany), SGS SA (Switzerland), WuXi AppTec (China), and Eurofins Scientific (Luxembourg). The key players in this market are focusing on strategic expansions, partnerships, and product launches and approvals to expand their presence in the market.

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[itssashasharma]

Global Biologics Safety Testing Market worth $ 6.2 billion : Emerging markets offer lucrative opportunities

This market research study involved the extensive use of secondary sources, directories, and databases to identify and collect information useful for this technical, market-oriented, and financial study of the global biologics safety testing market. In-depth interviews were conducted with various primary respondents, including key industry participants, subject-matter experts (SMEs), C-level executives of key market players, and industry consultants, among other experts, to obtain and verify critical qualitative and quantitative information and to assess market prospects.

According to the new market research report “Biologics Safety Testing Market by Product & Service (Consumables, Instrument, Services), Application (Vaccine, Monoclonal Antibodies, Blood products, Cell & Gene Therapy Products), Test Type (Endotoxin, Myoplasm, Sterility Test) – Global Forecast to 2026″, published by MarketsandMarkets™, the global market is projected to reach USD 6.2 billion by 2026 from USD 3.4 billion in 2021, at a CAGR of 12.4% during the forecast period. The growth of the global biologics safety testing market is driven by factors such as the growth in the biologics and biosimilars markets, growing concerns over cell culture contamination, and rising biopharmaceuticals R&D activities and investments. In addition, emerging markets and increasing biopharmaceutical outsourcing are expected to provide significant growth opportunities for players in the Biologics safety testing market. Browse in-depth TOC on “Biologics Safety Testing Market” 142 – Tables 42 – Figures 185 – Pages Download PDF Brochure: https://www.marketsandmarkets.com/pdfdownloadNew.asp?id=34624144 The growth of the global biologics safety market is driven by factors such as the growth in the biologics and biosimilars markets, growing concerns over cell culture contamination, and rising biopharmaceuticals R&D activities and investments. COVID-19 is an infectious disease caused by the most recently discovered novel coronavirus. Largely unknown before the outbreak began in Wuhan (China) in December 2019, COVID-19 has moved from a regional crisis to a global pandemic. The World Health Organization (WHO) officially declared the outbreak of COVID-19 a pandemic. A mix of established pharmaceutical and biopharmaceutical companies, along with the players of the Biologics safety testing market, have stepped forward to contribute to worldwide research efforts by providing biologics safety testing for developing safety test kits and testing for treatments and vaccines manufacturing that target the infection caused by the novel Coronavirus. The residual host-cell proteins and DNA detection tests segment accounted for the largest share of the Biologics Safety Testing market in 2020. Based on test type, the market is segmented into residual host-cell proteins and DNA detection tests, endotoxin tests, sterility tests, mycoplasma tests, bioburden tests, and virus safety tests. In 2020, the residual host-cell proteins and DNA detection tests segment accounted for the largest market share. The rising demand for residual HCP and DNA detection tests for recombinant proteins and increasing focus on the quality of drugs are the major factors driving the growth of this segment. The monoclonal antibodies manufacturing segment accounted for the largest market share of the market in 2020. Based on application, the biologics safety testing market is segmented into monoclonal antibodies manufacturing, vaccines manufacturing, blood and blood products manufacturing, cellular and gene therapy products manufacturing, and other applications. In 2020, the monoclonal antibodies manufacturing segment accounted for the largest market share. The large share of this segment can be attributed to the rising prevalence of diseases and increasing government initiatives for the development of monoclonal antibody drugs. Request Sample Pages: https://www.marketsandmarkets.com/requestsampleNew.asp?id=34624144 The Asia Pacific region is the fastest-growing region of the Biologics safety testing market in 2020. The Asia Pacific market is projected to witness the highest growth rate during the forecast period, primarily due to the expansion of key market players in emerging Asia Pacific countries, increasing expenditure on life science research, and the increasing trend of pharmaceutical outsourcing to Asia Pacific countries. Prominent players in the biologics safety testing market are Charles River Laboratories, Inc. (US), Lonza (Switzerland), Thermo Fisher Scientific, Inc. (US), Merck KGaA (Germany), SGS SA (Switzerland), WuXi AppTec (China), and Eurofins

Scientific (Luxembourg). The key players in this market are focusing on strategic expansions, partnerships, and product launches and approvals to expand their presence in the market. Browse Adjacent Markets: Biotechnology Market Research Reports & Consulting Browse Related Reports: Mycoplasma Testing Market by Product & Service (Assays, Kits, Reagents), Technique (NAT, ELISA, Staining), Application (Cell Line, End of Production Testing), End User (Biopharmaceutical, Cell Banks, CROs), Region – Global Forecast to 2025 https://www.marketsandmarkets.com/Market-Reports/mycoplasma-testing-market-136509856.html Pyrogen Testing Market by Product & Service (Assays, Kits, Reagents, Instruments, Services), Test Type (LAL, Chromogenic, Turbidimetric, Gel Clot, In Vitro, Rabbit), End User (Pharmaceutical, Biotechnology, Medical Device), Region – Global Forecast to 2025 https://www.marketsandmarkets.com/Market-Reports/pyrogen-testing-market-255266155.html About MarketsandMarkets™ MarketsandMarkets™ provides quantified B2B research on 30,000 high growth niche opportunities/threats which will impact 70% to 80% of worldwide companies’ revenues. Currently servicing 7500 customers worldwide including 80% of global Fortune 1000 companies as clients. Almost 75,000 top officers across eight industries worldwide approach MarketsandMarkets™ for their painpoints around revenues decisions. Our 850 fulltime analyst and SMEs at MarketsandMarkets™ are tracking global high growth markets following the “Growth Engagement Model – GEM”. The GEM aims at proactive collaboration with the clients to identify new opportunities, identify most important customers, write “Attack, avoid and defend” strategies, identify sources of incremental revenues for both the company and its competitors. MarketsandMarkets™ now coming up with 1,500 MicroQuadrants (Positioning top players across leaders, emerging companies, innovators, strategic players) annually in high growth emerging segments. MarketsandMarkets™ is determined to benefit more than 10,000 companies this year for their revenue planning and help them take their innovations/disruptions early to the market by providing them research ahead of the curve. MarketsandMarkets’s flagship competitive intelligence and market research platform, “Knowledge Store” connects over 200,000 markets and entire value chains for deeper understanding of the unmet insights along with market sizing and forecasts of niche markets. Contact: Mr. Aashish Mehra MarketsandMarkets™ INC. 630 Dundee Road Suite 430 Northbrook, IL 60062 USA: +1-888-600-6441 Email: sales@marketsandmarkets.com Research Insight: https://www.marketsandmarkets.com/ResearchInsight/biologics-safety-testing-market.asp Visit Our Web Site: https://www.marketsandmarkets.com Content Source: https://www.marketsandmarkets.com/PressReleases/biologics-safety-testing.asp