The document discusses how HIV home test kits work. Recent advances have made it possible for individuals to test for HIV in the privacy of their own home. The test kits are highly accurate and easy to use. They detect antibodies produced by the body in response to HIV, not the virus itself. It can take 4-12 weeks to develop antibodies after exposure, so the tests are most effective after this window period. The test involves pricking your finger for a blood sample, collecting drops of blood on the test strip, adding diluent, and waiting for a +, - or failed result to appear.
"Global HIV Vaccine Market Future Outlook" Report Highlights:
Introduction to HIV Vaccines
Issues Related to the Development of HIV Vaccines
Parameters for Successful Commercialization of HIV Vaccines
Global HIV Vaccines Market Opportunity Analysis
Global HIV Vaccine Clinical Pipeline by Company & Phase
Global HIV Vaccine Clinical Pipeline: 100 Vaccines
Majority Vaccine in Preclinical Phase: 42 Vaccines
The document discusses how to carry out an HIV home test using a test kit. It explains that HIV home test kits test for HIV antibodies in the blood and are readily available online from suppliers like Head Start Testing. It emphasizes the importance of using a test kit that is ISO and GMP certified to ensure accuracy and consistency. It also notes that Head Start Testing protects user privacy by using generic payment processing and discreet packaging and shipping. Finally, it describes how to use the test kit, which involves collecting a blood sample with a lancet, placing it in the test cartridge along with diluent, and reading the results within 1-2 minutes.
Poster prepared by Elise Schieck, Caroline Fossum, Bernt Hjertner and Claudia Lutzelschwab for the Virtual Livestock CRP Planning Meeting, 8-17 June 2020
Medicaltex has been proven to have antimicrobial properties according to the ASTM E 21-49 international standard, with testing confirming it prevents 99.99% of microbe formation. Medicaltex's antimicrobial agent and features are approved by several international laboratories and regulatory bodies. Tests show bacteria cannot adapt to Medicaltex due to its physical impact on cutting bacterial cell membranes.
Advancing Agrigenomic Discoveries with Sequencing and GWAS ResearchGolden Helix Inc
Agrigenomic research is difficult enough without having to coerce software designed for human genetics to work with the plant or animal species you're studying. Not anymore.
In this webcast, Greta Linse Peterson will present updated workflows in SNP & Variation Suite 8 (SVS) and GenomeBrowse for agricultural genetic research. SVS includes a robust suite of analytical tools and a revolutionary genome browser in one program to support a wide-variety of species including plant, animal, and parasites. New tools make it easy to adjust for inbreeding and incomplete pedigrees, making it even easier than before to identify variants related to pest and disease resistance, increased feed efficiency, milk production, and more. Topics to be covered include: supported file formats for importing data (including imputation sources like FindHap, Fimpute, and Impute2), comprehensive sequencing and GWAS workflows to take your analysis from QA to finding putative variants or SNPs of interest, common pitfalls to avoid and precautions when working with agrigenomic data, and visualizing results seamlessly in an integrated genome browser.
Bharat Biotech’s research stems from the need to innovate and the necessity to address public health requirements of the developing nations, while adhering to IPR. Our business model is to support the advancement of technologies through strong collaborative research, and simultaneously support the establishment of strong innovative technology platforms for intellectual property reputed driven enterprise R&D.
Antivirus software testing for the new milleniumUltraUploader
This document discusses the need for standardized testing of antivirus software to properly evaluate claims by vendors of providing "faster, better, cheaper" protection. It outlines the current state of antivirus testing, including certification programs run by ICSA, Westcoast Labs, and universities. The tests evaluate detection of viruses in the wild and ability to disinfect. The document argues for a functional approach to testing that is not specific to any vendor or product.
The document discusses how HIV home test kits work. Recent advances have made it possible for individuals to test for HIV in the privacy of their own home. The test kits are highly accurate and easy to use. They detect antibodies produced by the body in response to HIV, not the virus itself. It can take 4-12 weeks to develop antibodies after exposure, so the tests are most effective after this window period. The test involves pricking your finger for a blood sample, collecting drops of blood on the test strip, adding diluent, and waiting for a +, - or failed result to appear.
"Global HIV Vaccine Market Future Outlook" Report Highlights:
Introduction to HIV Vaccines
Issues Related to the Development of HIV Vaccines
Parameters for Successful Commercialization of HIV Vaccines
Global HIV Vaccines Market Opportunity Analysis
Global HIV Vaccine Clinical Pipeline by Company & Phase
Global HIV Vaccine Clinical Pipeline: 100 Vaccines
Majority Vaccine in Preclinical Phase: 42 Vaccines
The document discusses how to carry out an HIV home test using a test kit. It explains that HIV home test kits test for HIV antibodies in the blood and are readily available online from suppliers like Head Start Testing. It emphasizes the importance of using a test kit that is ISO and GMP certified to ensure accuracy and consistency. It also notes that Head Start Testing protects user privacy by using generic payment processing and discreet packaging and shipping. Finally, it describes how to use the test kit, which involves collecting a blood sample with a lancet, placing it in the test cartridge along with diluent, and reading the results within 1-2 minutes.
Poster prepared by Elise Schieck, Caroline Fossum, Bernt Hjertner and Claudia Lutzelschwab for the Virtual Livestock CRP Planning Meeting, 8-17 June 2020
Medicaltex has been proven to have antimicrobial properties according to the ASTM E 21-49 international standard, with testing confirming it prevents 99.99% of microbe formation. Medicaltex's antimicrobial agent and features are approved by several international laboratories and regulatory bodies. Tests show bacteria cannot adapt to Medicaltex due to its physical impact on cutting bacterial cell membranes.
Advancing Agrigenomic Discoveries with Sequencing and GWAS ResearchGolden Helix Inc
Agrigenomic research is difficult enough without having to coerce software designed for human genetics to work with the plant or animal species you're studying. Not anymore.
In this webcast, Greta Linse Peterson will present updated workflows in SNP & Variation Suite 8 (SVS) and GenomeBrowse for agricultural genetic research. SVS includes a robust suite of analytical tools and a revolutionary genome browser in one program to support a wide-variety of species including plant, animal, and parasites. New tools make it easy to adjust for inbreeding and incomplete pedigrees, making it even easier than before to identify variants related to pest and disease resistance, increased feed efficiency, milk production, and more. Topics to be covered include: supported file formats for importing data (including imputation sources like FindHap, Fimpute, and Impute2), comprehensive sequencing and GWAS workflows to take your analysis from QA to finding putative variants or SNPs of interest, common pitfalls to avoid and precautions when working with agrigenomic data, and visualizing results seamlessly in an integrated genome browser.
Bharat Biotech’s research stems from the need to innovate and the necessity to address public health requirements of the developing nations, while adhering to IPR. Our business model is to support the advancement of technologies through strong collaborative research, and simultaneously support the establishment of strong innovative technology platforms for intellectual property reputed driven enterprise R&D.
Antivirus software testing for the new milleniumUltraUploader
This document discusses the need for standardized testing of antivirus software to properly evaluate claims by vendors of providing "faster, better, cheaper" protection. It outlines the current state of antivirus testing, including certification programs run by ICSA, Westcoast Labs, and universities. The tests evaluate detection of viruses in the wild and ability to disinfect. The document argues for a functional approach to testing that is not specific to any vendor or product.
The first section of Part III will cover the most immediate healthcare response - which is to test and diagnose patients for COVID-19, to get a clear picture on the extent of the spread of infection. It also covers the current technologies used in diagnostics: RT-PCR, LAMP, Lateral Flow and ELISA. It would also highlight key companies and comparison of the technologies involved.
NanoViricides is developing nanomedicine-based drugs to treat various viral diseases like influenza, HIV, hepatitis C, and Ebola. The company has 9 drug candidates in development that have shown safety and efficacy in animal studies. NanoViricides' first drug to enter human trials will be FluCide for influenza, which completely protected animals against lethal viral exposure without toxicity.
Health Advances Demystifying COVID Testing - 4th Edition.pdfHealth Advances
• As we enter the endemic phase of COVID-19, we wanted to share our final edition of Demystifying COVID-19 Testing. In this edition, we provide an update on testing dynamics and share our assessment of the impact on the industry and our predictions for the future.
This report analyzes the worldwide markets for HIV/AIDS Testing in US$ Million by the following product segments: HIV/AIDS Screening Tests, HIV/AIDS Confirmatory Tests, and HIV/AIDS Monitoring Tests. The report provides separate comprehensive analytics for the US, Canada, Japan, Europe, Asia-Pacific, Latin America, and Rest of World. Annual estimates and forecasts are provided for the period 2007 through 2015. A seven-year historic analysis is also provided for these markets.The report profiles 63 companies including many key and niche players such as Abbott Laboratories Inc., Abbott Molecular Inc., Adaltis S.r.l., Biom
Current Status and Future Perspective of Rapid Diagnostic Kits Vaccine agains...ijtsrd
Coronavirus disease 2019 COVID 19 , which causes serious respiratory illness such as pneumonia and lung failure, was first reported in Wuhan, the capital of Hubei, China. The etiological agent of COVID 19 has been confirmed as a novel coronavirus, now known as severe acute respiratory syndrome coronavirus 2 SARS CoV 2 , which is most likely originated from zoonotic coronaviruses, like SARS CoV, which emerged in 2002. Rapid diagnostics, vaccines and therapeutics are important interventions for the management of the 2019 novel coronavirus 2019 nCoV outbreak. Currently, various diagnostic kits to test for COVID 19 are available and several repurposing therapeutics for COVID 19 have shown to be clinically effective. In addition, global institutions and companies have begun to develop vaccines for the prevention of COVID 19. Here, we review the current status of, diagnosis, and vaccine development for COVID 19. M A Nandedkar | R A Shinde | S S Bansode "Current Status and Future Perspective of Rapid Diagnostic Kits / Vaccine against COVID-19" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-4 , June 2020, URL: https://www.ijtsrd.com/papers/ijtsrd30977.pdf Paper Url :https://www.ijtsrd.com/pharmacy/analytical-chemistry/30977/current-status-and-future-perspective-of-rapid-diagnostic-kits--vaccine-against-covid19/m-a-nandedkar
JPS Global Group, which offers the best Covid-19 Test Kits in Australia, has submitted this PDF. JPS Global Group sells TGA-approved Rapid Antigen Tests and, more significantly, assists companies in developing and implementing a compliance and efficient testing strategy. For additional information, please visit our website.
Covid 19, vaccine and it's development process - Group 1XinLu53
The document summarizes COVID-19, the development of vaccines for COVID-19, and compares the traditional vaccine development process to the COVID-19 vaccine development process. Specifically:
1) It provides background on COVID-19, describing the virus, symptoms, and transmission routes.
2) It discusses the global effort to develop COVID-19 vaccines, with over 157 candidates in development as of June 2020 and 16 in clinical trials.
3) It summarizes the AstraZeneca/Oxford AZD1222 vaccine, how it works, and results from Phase 1/2 clinical trials showing an immune response.
4) It compares the traditional long vaccine development process, taking 6-20 years, to the accelerated
There are an estimated 33.3 million people living with HIV (the virus which causes AIDS) worldwide and approximately 2.6 million people are newly-infected each year. While the Asian and African regions account for more than 90% of the HIV-infected population (with the highest number in Sub-Saharan Africa), the U.S. and European regions make up greater than 60% of the HIV testing market. This TriMark Publications report provides a comprehensive examination of the HIV/AIDS testing market, a specific segment of the in vitro diagnostics (IVD) market as it relates to infectious diseases. It examines the available and emerging technologies being utilized by the HIV testing field, defines the dollar volume of sales'both in the U.S. and worldwide'and analyzes the factors that influence the size and growth of the market. The chief HIV testing assays, i.e., predictive, screening, prognostic, monitoring, pharmacogenomic and theranostic, are covered thoroughly, as are high-growth applications in different clinical diagnostic areas and expanding markets, such as employee screening, emergency medicine and satellite clinic testing. Additionally, this analysis covers the following areas in details: enzyme-linked immunosorbent assay (ELISA), antibody/p24 antigen test (fourth-generation test), Western blot assay, line immunoassays, indirect fluorescent antibody (IFA) assay, nucleic acid tests for infectious diseases, and the emerging technologies related to HIV and AIDS diagnosis. Moreover, this study also provides a thorough analysis of the companies known to be marketing, manufacturing or developing HIV testing products, as well as provides detailed tables and figures covering HIV testing markets around the globe.
In this section of the coronavirus pandemic series, we discuss the current capacity of local healthcare systems and the need for effective treatment options as well as the pathogenesis of the coronavirus. Current treatment options include RNA, monoclonal antibodies (mAb), antibodies, convalescent plasma, and others. Critical stage implications such as cytokine storm and the need for immunomodulatory agents would also be discussed. Therapeutic pathways would are also compared.
This document provides an overview of SARS-CoV-2 testing. It describes the different types of diagnostic tests used in the COVID-19 response, including molecular tests that detect the virus's genetic material, antigen tests that detect viral proteins, and antibody tests that detect antibodies produced in response to infection. Accurate and rapid diagnostic testing is essential for confirming active infections, screening suspected cases, and determining the true extent of outbreaks. The document explains key terms like antigens and antibodies and where the different types of tests can be used, such as laboratories or point-of-care settings.
The document proposes establishing a joint venture company between Bioland LTD and a Vietnamese partner, Nam-Khoa Biotek LTD, to produce rapid diagnostic tests in Vietnam. There is increasing demand for such tests in countries like Vietnam to detect diseases like malaria, hepatitis, HIV, and others. The joint venture would manufacture tests for diseases locally to sell in Vietnam and abroad, leveraging Bioland's expertise in research and development and manufacturing and Nam-Khoa's facilities, sales network, and regulatory knowledge in Vietnam. The proposal outlines contributions, governance, production plans, timelines, and profit distribution between the partners.
COVID-19 and the flu share common symptoms, making it challenging to distinguish between the two without proper testing. Traditional testing methods often lead to delays, hindering quick decision-making in critical situations. Covid flu rapid test is the key to overcoming these challenges.
Population-scale and rapid testing for SARS-CoV-2 continues to be a priority for several parts of the world. We revisit the in vitro technology platforms for COVID-19 testing and diagnostics—molecular tests and rapid antigen tests, serology or antibody tests, and tests for the management of COVID-19 patients. Within each category of tests, we review the commercialized testing platforms, their analyzing systems, specimen collection protocols, testing methodologies, supply chain logistics, and related attributes. Our discussion is essentially focused on test products that have been granted emergency use authorization by the FDA to detect and diagnose COVID-19 infections. Different strategies for scaled-up and faster screening are covered here, such as pooled testing, screening programs, and surveillance testing. The near-term challenges lie in detecting subtle infectivity profiles, mapping the transmission dynamics of new variants, lowering the cost for testing, training a large healthcare workforce, and providing test kits for the masses. Through this review, we try to understand the feasibility of universal access to COVID-19 testing and diagnostics in the near future while being cognizant of the implicit tradeoffs during the development and distribution cycles of new testing platforms.
EVE198 Fall2020 "Covid Mass Testing" Class 8 VaccinesJonathan Eisen
This document discusses a class on vaccines for COVID-19. It covers topics like vaccine development, current candidate vaccines, challenges with vaccine distribution, and how vaccines are being assessed for safety, effectiveness, costs and production feasibility. Over 100 vaccine candidates are in development using platforms like DNA, RNA, viral vectors and inactivated viruses. Efforts like Operation Warp Speed are coordinating development of nucleic acid, viral vector and protein subunit vaccines. Distribution challenges include vaccine production, storage and logistics, number of doses required, and overcoming vaccine nationalism and hesitancy.
HealthBIO 2021_PerkinElmer, leading with innovation - from COVID success into...Business Turku
This document provides an overview of PerkinElmer, a company focused on diagnostics, life sciences, food, and applied markets. It discusses their mission of innovating for a healthier world, with over 80 years of innovations including a COVID-19 PCR kit launched in 2020. The company's diagnostics segment focuses on reproductive health, immunoassays, and applied genomics. PerkinElmer has global capabilities across molecular diagnostics, imaging, automation, and more. It is pursuing growth in areas like single-cell analysis, therapeutics, digital solutions, and decentralized testing. The company's strategy focuses on detection, decentralization, and digitization to drive profitable growth.
This document summarizes a presentation on using next generation sequencing (NGS) to improve virus and viroid detection for plants in post-entry quarantine (PEQ). Current PEQ diagnostic methods are slow and can miss pathogens. The presentation describes how NGS allows rapid and reliable detection of viruses without prior knowledge. A project found viruses in 68% of plant samples tested using NGS compared to traditional methods. NGS could reduce PEQ time from over 2 years to 6-12 months. Industry representatives expressed support but want more validation before fully adopting NGS for high-stakes pathogen testing and certification schemes. The project aims to provide more evidence and training to facilitate adoption of NGS for improving plant biosecurity.
"Global HIV Vaccine Market Future Outlook" Report Highlights:
Introduction to HIV Vaccines
Issues Related to the Development of HIV Vaccines
Parameters for Successful Commercialization of HIV Vaccines
Global HIV Vaccines Market Opportunity Analysis
Global HIV Vaccine Clinical Pipeline by Company & Phase
Global HIV Vaccine Clinical Pipeline: 100 Vaccines
Majority Vaccine in Preclinical Phase: 42 Vaccines
In this webinar, you will learn:
Trends in vaccine manufacturing
Innovative solutions in facility design
Case studies and proposals for future vaccine factories
Considerations while setting up Quality Management Systems (QMSs)
How validation helps accelerate regulatory approval
Detailed description:
How we see vaccine manufacturing evolving due to the COVID-19 pandemic, how could it further transform, and what are some solutions we can incorporate to prepare ourselves for next-generation facilities?
The unprecedented COVID-19 pandemic has driven significant tech acceleration around the world, including methods of vaccine manufacturing. Together with the concept of Bioprocessing 4.0, digital biomanufacturing enables centralized orchestration of production process and data management, and a "Facility of the Future" characterized by intensified, continuous, predictive, and autonomous operations. In this presentation, we will explore trends in vaccine manufacturing, including fully single-use processes, closed processing, modular facilities, and platform manufacturing. We will also discuss some key considerations when setting up Quality Management Systems for novel facilities, and how to speed up regulatory approval through best practices in facility validation.
In this webinar, you will learn:
Trends in vaccine manufacturing
Innovative solutions in facility design
Case studies and proposals for future vaccine factories
Considerations while setting up Quality Management Systems (QMSs)
How validation helps accelerate regulatory approval
Detailed description:
How we see vaccine manufacturing evolving due to the COVID-19 pandemic, how could it further transform, and what are some solutions we can incorporate to prepare ourselves for next-generation facilities?
The unprecedented COVID-19 pandemic has driven significant tech acceleration around the world, including methods of vaccine manufacturing. Together with the concept of Bioprocessing 4.0, digital biomanufacturing enables centralized orchestration of production process and data management, and a "Facility of the Future" characterized by intensified, continuous, predictive, and autonomous operations. In this presentation, we will explore trends in vaccine manufacturing, including fully single-use processes, closed processing, modular facilities, and platform manufacturing. We will also discuss some key considerations when setting up Quality Management Systems for novel facilities, and how to speed up regulatory approval through best practices in facility validation.
Whiteboard2Boardroom collaborates with more than 21 research institutions, hospitals and corporation to move technologies out of research labs into the marketplace.
Whiteboard2Boardroom collaborates with more than 21 research institutions, hospitals and corporation to move technologies out of research labs into the marketplace.
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The first section of Part III will cover the most immediate healthcare response - which is to test and diagnose patients for COVID-19, to get a clear picture on the extent of the spread of infection. It also covers the current technologies used in diagnostics: RT-PCR, LAMP, Lateral Flow and ELISA. It would also highlight key companies and comparison of the technologies involved.
NanoViricides is developing nanomedicine-based drugs to treat various viral diseases like influenza, HIV, hepatitis C, and Ebola. The company has 9 drug candidates in development that have shown safety and efficacy in animal studies. NanoViricides' first drug to enter human trials will be FluCide for influenza, which completely protected animals against lethal viral exposure without toxicity.
Health Advances Demystifying COVID Testing - 4th Edition.pdfHealth Advances
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This report analyzes the worldwide markets for HIV/AIDS Testing in US$ Million by the following product segments: HIV/AIDS Screening Tests, HIV/AIDS Confirmatory Tests, and HIV/AIDS Monitoring Tests. The report provides separate comprehensive analytics for the US, Canada, Japan, Europe, Asia-Pacific, Latin America, and Rest of World. Annual estimates and forecasts are provided for the period 2007 through 2015. A seven-year historic analysis is also provided for these markets.The report profiles 63 companies including many key and niche players such as Abbott Laboratories Inc., Abbott Molecular Inc., Adaltis S.r.l., Biom
Current Status and Future Perspective of Rapid Diagnostic Kits Vaccine agains...ijtsrd
Coronavirus disease 2019 COVID 19 , which causes serious respiratory illness such as pneumonia and lung failure, was first reported in Wuhan, the capital of Hubei, China. The etiological agent of COVID 19 has been confirmed as a novel coronavirus, now known as severe acute respiratory syndrome coronavirus 2 SARS CoV 2 , which is most likely originated from zoonotic coronaviruses, like SARS CoV, which emerged in 2002. Rapid diagnostics, vaccines and therapeutics are important interventions for the management of the 2019 novel coronavirus 2019 nCoV outbreak. Currently, various diagnostic kits to test for COVID 19 are available and several repurposing therapeutics for COVID 19 have shown to be clinically effective. In addition, global institutions and companies have begun to develop vaccines for the prevention of COVID 19. Here, we review the current status of, diagnosis, and vaccine development for COVID 19. M A Nandedkar | R A Shinde | S S Bansode "Current Status and Future Perspective of Rapid Diagnostic Kits / Vaccine against COVID-19" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-4 , June 2020, URL: https://www.ijtsrd.com/papers/ijtsrd30977.pdf Paper Url :https://www.ijtsrd.com/pharmacy/analytical-chemistry/30977/current-status-and-future-perspective-of-rapid-diagnostic-kits--vaccine-against-covid19/m-a-nandedkar
JPS Global Group, which offers the best Covid-19 Test Kits in Australia, has submitted this PDF. JPS Global Group sells TGA-approved Rapid Antigen Tests and, more significantly, assists companies in developing and implementing a compliance and efficient testing strategy. For additional information, please visit our website.
Covid 19, vaccine and it's development process - Group 1XinLu53
The document summarizes COVID-19, the development of vaccines for COVID-19, and compares the traditional vaccine development process to the COVID-19 vaccine development process. Specifically:
1) It provides background on COVID-19, describing the virus, symptoms, and transmission routes.
2) It discusses the global effort to develop COVID-19 vaccines, with over 157 candidates in development as of June 2020 and 16 in clinical trials.
3) It summarizes the AstraZeneca/Oxford AZD1222 vaccine, how it works, and results from Phase 1/2 clinical trials showing an immune response.
4) It compares the traditional long vaccine development process, taking 6-20 years, to the accelerated
There are an estimated 33.3 million people living with HIV (the virus which causes AIDS) worldwide and approximately 2.6 million people are newly-infected each year. While the Asian and African regions account for more than 90% of the HIV-infected population (with the highest number in Sub-Saharan Africa), the U.S. and European regions make up greater than 60% of the HIV testing market. This TriMark Publications report provides a comprehensive examination of the HIV/AIDS testing market, a specific segment of the in vitro diagnostics (IVD) market as it relates to infectious diseases. It examines the available and emerging technologies being utilized by the HIV testing field, defines the dollar volume of sales'both in the U.S. and worldwide'and analyzes the factors that influence the size and growth of the market. The chief HIV testing assays, i.e., predictive, screening, prognostic, monitoring, pharmacogenomic and theranostic, are covered thoroughly, as are high-growth applications in different clinical diagnostic areas and expanding markets, such as employee screening, emergency medicine and satellite clinic testing. Additionally, this analysis covers the following areas in details: enzyme-linked immunosorbent assay (ELISA), antibody/p24 antigen test (fourth-generation test), Western blot assay, line immunoassays, indirect fluorescent antibody (IFA) assay, nucleic acid tests for infectious diseases, and the emerging technologies related to HIV and AIDS diagnosis. Moreover, this study also provides a thorough analysis of the companies known to be marketing, manufacturing or developing HIV testing products, as well as provides detailed tables and figures covering HIV testing markets around the globe.
In this section of the coronavirus pandemic series, we discuss the current capacity of local healthcare systems and the need for effective treatment options as well as the pathogenesis of the coronavirus. Current treatment options include RNA, monoclonal antibodies (mAb), antibodies, convalescent plasma, and others. Critical stage implications such as cytokine storm and the need for immunomodulatory agents would also be discussed. Therapeutic pathways would are also compared.
This document provides an overview of SARS-CoV-2 testing. It describes the different types of diagnostic tests used in the COVID-19 response, including molecular tests that detect the virus's genetic material, antigen tests that detect viral proteins, and antibody tests that detect antibodies produced in response to infection. Accurate and rapid diagnostic testing is essential for confirming active infections, screening suspected cases, and determining the true extent of outbreaks. The document explains key terms like antigens and antibodies and where the different types of tests can be used, such as laboratories or point-of-care settings.
The document proposes establishing a joint venture company between Bioland LTD and a Vietnamese partner, Nam-Khoa Biotek LTD, to produce rapid diagnostic tests in Vietnam. There is increasing demand for such tests in countries like Vietnam to detect diseases like malaria, hepatitis, HIV, and others. The joint venture would manufacture tests for diseases locally to sell in Vietnam and abroad, leveraging Bioland's expertise in research and development and manufacturing and Nam-Khoa's facilities, sales network, and regulatory knowledge in Vietnam. The proposal outlines contributions, governance, production plans, timelines, and profit distribution between the partners.
COVID-19 and the flu share common symptoms, making it challenging to distinguish between the two without proper testing. Traditional testing methods often lead to delays, hindering quick decision-making in critical situations. Covid flu rapid test is the key to overcoming these challenges.
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EVE198 Fall2020 "Covid Mass Testing" Class 8 VaccinesJonathan Eisen
This document discusses a class on vaccines for COVID-19. It covers topics like vaccine development, current candidate vaccines, challenges with vaccine distribution, and how vaccines are being assessed for safety, effectiveness, costs and production feasibility. Over 100 vaccine candidates are in development using platforms like DNA, RNA, viral vectors and inactivated viruses. Efforts like Operation Warp Speed are coordinating development of nucleic acid, viral vector and protein subunit vaccines. Distribution challenges include vaccine production, storage and logistics, number of doses required, and overcoming vaccine nationalism and hesitancy.
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This document provides an overview of PerkinElmer, a company focused on diagnostics, life sciences, food, and applied markets. It discusses their mission of innovating for a healthier world, with over 80 years of innovations including a COVID-19 PCR kit launched in 2020. The company's diagnostics segment focuses on reproductive health, immunoassays, and applied genomics. PerkinElmer has global capabilities across molecular diagnostics, imaging, automation, and more. It is pursuing growth in areas like single-cell analysis, therapeutics, digital solutions, and decentralized testing. The company's strategy focuses on detection, decentralization, and digitization to drive profitable growth.
This document summarizes a presentation on using next generation sequencing (NGS) to improve virus and viroid detection for plants in post-entry quarantine (PEQ). Current PEQ diagnostic methods are slow and can miss pathogens. The presentation describes how NGS allows rapid and reliable detection of viruses without prior knowledge. A project found viruses in 68% of plant samples tested using NGS compared to traditional methods. NGS could reduce PEQ time from over 2 years to 6-12 months. Industry representatives expressed support but want more validation before fully adopting NGS for high-stakes pathogen testing and certification schemes. The project aims to provide more evidence and training to facilitate adoption of NGS for improving plant biosecurity.
"Global HIV Vaccine Market Future Outlook" Report Highlights:
Introduction to HIV Vaccines
Issues Related to the Development of HIV Vaccines
Parameters for Successful Commercialization of HIV Vaccines
Global HIV Vaccines Market Opportunity Analysis
Global HIV Vaccine Clinical Pipeline by Company & Phase
Global HIV Vaccine Clinical Pipeline: 100 Vaccines
Majority Vaccine in Preclinical Phase: 42 Vaccines
In this webinar, you will learn:
Trends in vaccine manufacturing
Innovative solutions in facility design
Case studies and proposals for future vaccine factories
Considerations while setting up Quality Management Systems (QMSs)
How validation helps accelerate regulatory approval
Detailed description:
How we see vaccine manufacturing evolving due to the COVID-19 pandemic, how could it further transform, and what are some solutions we can incorporate to prepare ourselves for next-generation facilities?
The unprecedented COVID-19 pandemic has driven significant tech acceleration around the world, including methods of vaccine manufacturing. Together with the concept of Bioprocessing 4.0, digital biomanufacturing enables centralized orchestration of production process and data management, and a "Facility of the Future" characterized by intensified, continuous, predictive, and autonomous operations. In this presentation, we will explore trends in vaccine manufacturing, including fully single-use processes, closed processing, modular facilities, and platform manufacturing. We will also discuss some key considerations when setting up Quality Management Systems for novel facilities, and how to speed up regulatory approval through best practices in facility validation.
In this webinar, you will learn:
Trends in vaccine manufacturing
Innovative solutions in facility design
Case studies and proposals for future vaccine factories
Considerations while setting up Quality Management Systems (QMSs)
How validation helps accelerate regulatory approval
Detailed description:
How we see vaccine manufacturing evolving due to the COVID-19 pandemic, how could it further transform, and what are some solutions we can incorporate to prepare ourselves for next-generation facilities?
The unprecedented COVID-19 pandemic has driven significant tech acceleration around the world, including methods of vaccine manufacturing. Together with the concept of Bioprocessing 4.0, digital biomanufacturing enables centralized orchestration of production process and data management, and a "Facility of the Future" characterized by intensified, continuous, predictive, and autonomous operations. In this presentation, we will explore trends in vaccine manufacturing, including fully single-use processes, closed processing, modular facilities, and platform manufacturing. We will also discuss some key considerations when setting up Quality Management Systems for novel facilities, and how to speed up regulatory approval through best practices in facility validation.
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Whiteboard2Boardroom collaborates with more than 21 research institutions, hospitals and corporation to move technologies out of research labs into the marketplace.
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Whiteboard2Boardroom collaborates with more than 21 research institutions, hospitals and corporation to move technologies out of research labs into the marketplace.
The document summarizes a proposed solution to improve the effectiveness of disposable medical gowns. Current disposable gowns do not meet FDA regulations as they gap and sag, exposing healthcare workers' clothing and risking contamination. The proposed solution extends the gown material up the neck to prevent gaps. This would make disposable gowns compliant with regulations while providing an inexpensive, simple solution. Further development requires demonstrating current gowns' ineffectiveness, such as with a fluorescent particle video test, and pursuing partnerships with manufacturers or the FDA to drive regulatory changes ensuring gown protection.
Non-Resistant Antimicrobial Therapy: Treating Superbugs That Cause Nosocomial...kphodel
This document discusses a new treatment for hospital-acquired pneumonia (HAP) using a combination of SynAmp, a non-antibiotic compound that enhances antibiotic potency, and an antibiotic. HAP is a major problem with high mortality and increasing antibiotic resistance. The combination therapy is a first-line treatment for HAP that is dosed once daily and shows no resistance after 30 days. It has intellectual property protection and competitive advantages over current treatments. With expedited regulatory pathways, the company aims to launch the primary HAP indication with $200 million in annual sales and expand to other infections. Funding is sought to further develop the pre-clinical candidate.
This webinar aims to attract entrepreneurs and corporations to license two technologies presented: the Mizzou BioJoint Flex knee range of motion device. The webinar will include 10-minute presentations on each technology and a question period. The BioJoint Flex addresses knee arthrofibrosis by providing a gentle, prolonged stretch at home or in a clinic. It has undergone initial clinical trials demonstrating benefits in flexion, function, pain and satisfaction over physical therapy. Further development needs include finding a licensing partner for manufacturing and marketing, finalizing the patient and pro versions, pursuing 510k clearance, and commercialization. The presentation provides details on intellectual property, development stage, clinical results, market opportunity, competition, and the development team.
The webinar aims to (1) attract entrepreneurs to license technologies to start companies, (2) attract corporations to license technologies for new products, and (3) solicit input on commercial viability. The agenda includes a schedule, two 10-minute technology presentations on medical devices to diagnose swallowing disorders, and a question period. The first device, Down the Hatch, provides objective data from endoscopy videos to diagnose and prevent aspiration pneumonia. The second, Tongue Twister, is a mobile app that provides objective data on speech and swallowing tasks to assess patients. Both technologies are patent-pending and seeking start-up partners for further development and commercialization.
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Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kol...rightmanforbloodline
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Versio
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Does Over-Masturbation Contribute to Chronic Prostatitis.pptxwalterHu5
In some case, your chronic prostatitis may be related to over-masturbation. Generally, natural medicine Diuretic and Anti-inflammatory Pill can help mee get a cure.
2. What is the problem?
715,000 cases/day
While companies were working
on a rapid antigen test, COVID-19
infections were running wild
https://ourworldindata.org/covid-cases
3. What is the problem?
https://ourworldindata.org/covid-cases
SARS-CoV2
Genome
Sequenced
Deployment
of Rapid Ab
Test
While companies were working
on a rapid antigen test, COVID-19
infections were running wild
7 Month Development Time
4. What is the problem?
https://ourworldindata.org/covid-cases
Nucleotide-Based
Diagnostic
SARS-CoV2
Genome
Sequenced
1 Month Development Time
5. How does product/service solve problem?
Faster to develop
Simpler to use
Adaptable to new viruses
capture
reporter
Our Test Is:
6. What is the market use?
Highly demanded during new
infectious diseases
Absent from the market
Minimal competition
Early diagnostic test kits are:
7. What is the market use?
Highly demanded during new
infectious diseases
Absent from the market
Minimal competition
or
or
Early diagnostic test kits are:
Alternative Market Applications:
wide-market utility in research
labs
8. What competition exists?
• Antigen tests are the
gold standard for viral
testing (Abbott Labs,
etc.)
• However these take
months (~7) to develop
• RT-PCR testing is the
first viable testing done
for emerging diseases
• Results take days-to-
one week to return
• In the meantime…
9. What is the status of the intellectual property?
• Patent pending on Nucleotide-Based
Infectious Disease Diagnostic Test
• Patents in preparation:
– Nucleotide-Based Reporter Adaptors
– Amplification Reagent for Immunoassays
10. What is the stage of development?
-0.4
-0.2
0
0.2
0.4
0.6
0.8
1
1.2
1.4
positive
control
scrambled
target
negative
control
100nM 10nM 1nM 100pM
OD370
LOD for oligonucleotide ELISA
Early proof of principle tests
have been successful
Methods will be developed
for sample processing and
detection of physiological
concentrations of virus
11. What is needed for further development?
• Business Partner (CEO)
• Support for Preclinical
Development
• Clinical Connection for
Final Validation
• Equipment and
Consumables
• Scaling to Production
Editor's Notes
We were caught flat-footed by COVID-19. Even when we identified the organism causing the disease and sequenced its genome, we were still unable to engage a rapid testing regimen to do effective monitoring and contact tracing.
This led to the uncontrolled spread of disease across the globe
We were caught flat-footed by COVID-19. Even when we identified the organism causing the disease and sequenced its genome, we were still unable to engage a rapid testing regimen to do effective monitoring and contact tracing.
This led to the uncontrolled spread of disease across the globe
We were caught flat-footed by COVID-19. Even when we identified the organism causing the disease and sequenced its genome, we were still unable to engage a rapid testing regimen to do effective monitoring and contact tracing.
This led to the uncontrolled spread of disease across the globe
In addition to faster deployment, our nucleotide-based test would be easier to use, require less training, less equipment, and have faster turn-around time between test and result.
The COVID-19 diagnostic is just an example of an adaptive test capable of being used for numerous emerging infectious diseases. Furthermore, the development of this diagnostic has led to the invention of several related reagent types which could be used in numerous laboratory applications including Flow Cytometry, Western Blotting, and ELISAs.
The COVID-19 diagnostic is just an example of an adaptive test capable of being used for numerous emerging infectious diseases. Furthermore, the development of this diagnostic has led to the invention of several related reagent types which could be used in numerous laboratory applications including Flow Cytometry, Western Blotting, and ELISAs.
There is competition for this diagnostic. However, early-adaptable tests tend to take longer times and greater costs to process samples and provide results. Rapid, simple tests like the antibody test take many months to develop. This results in a window of opportunity for a simple, rapid test that can be developed early in an epidemic.
A provisional patent has been filed for the diagnostic test, while we are developing data to support additional applications for related products.
We have currently generated proof of principle data showing that both the concepts for the diagnostic test and the reagent labeling technology work well. Further development is required in developing the amplification reagent required to detect smaller concentrations of material as found in physiological samples. We are