This report provides an analysis of the product pipeline of AnaZyme, LLC, a diagnostic assay company focused on developing assays to detect biomarkers for the onset and progression of shock. The report details AnaZyme's three main pipeline products: a breath-based assay to detect volatile compounds for shock; a blood-based assay to detect specific enzymes; and a blood-based assay to detect the absence of specific compounds. All assays can be run on commercially available laboratory instruments. The report provides profiles of each pipeline product along with their status, descriptions, applications, and patent details. It aims to help readers understand AnaZyme's portfolio and competitive landscape to support business and market strategies.
Expert witness view of fda regulated companies - information trial attorneys ...Joshua Sharlin, Ph.D.
1. Learn an expert witness’s view about common problems and errors in the processes FDA requires
2. Understand how information is collected and reported in today’s FDA-regulated environment
3. Identify documents that add to a knowledgebase about the activities and results of FDA-regulated processes
Acid Indigestion / Heartburn/ Pyrosis Global Clinical Trials Review, H1, 2013
Summary
GlobalData's clinical trial report, 'Acid Indigestion / Heartburn/ Pyrosis Global Clinical Trials Review, H1, 2013" provides data on the Acid Indigestion / Heartburn/ Pyrosis clinical trial scenario. This report provides elemental information and data relating to the clinical trials on Acid Indigestion / Heartburn/ Pyrosis. It includes an overview of the trial numbers and their recruitment status as per the site of trial conduction across the globe. The databook offers a preliminary coverage of disease clinical trials by their phase, trial status, prominence of the sponsors and also provides briefing pertaining to the number of trials for the key drugs for treating Acid Indigestion / Heartburn/ Pyrosis. This report is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GlobalData's team of industry experts.Note: Certain sections in the report may be removed or altered based on the availability and relevance of data for the indicated disease.
Scope
- Data on the number of clinical trials conducted in North America, South and Central America, Europe, Middle-East and Africa and Asia-pacific and top five national contributions in each, along with the clinical trial scenario in BRIC nations - Clinical trial (complete and in progress) data by phase, trial status, subjects recruited and sponsor type- Listings of discontinued trials (suspended, withdrawn and terminated)
Reasons to buy
- Understand the dynamics of a particular indication in a condensed manner- Abridged view of the performance of the trials in terms of their status, recruitment, location, sponsor type and many more- Obtain discontinued trial listing for trials across the globe- Espy the commercial landscape of the major Universities / Institutes / Hospitals or Companies
Satisfying us and eu human factors requirements for inhaler devicesCambridge Consultants
HFE is an essential and integral part of the inhaler device development process. The process requirements are primarily based on the core principles of safety and effectiveness. The HFE processes for the FDA and EU submissions are largely harmonized, but there are some minor differences. It is important that manufacturers of inhaler devices understand the process clearly so that they can comply with the requirements. Following the HFE process does not only fulfil the regulatory requirements but also helps you to develop better products. This presentation provides the holistic view of the HFE process in a simple schematic way, however every project is different and the process should be tailored accordingly.
Making PrescriptionsPpersonal - Pharmacogenomics reports - Software in MedicineGDG Budapest
10 éven belül valóra válhatna az a még
kissé futurisztikusnak tűnő kép, hogy mindenkiről egy genetikai
polimorfizmus adattár áll rendelkezésre mondjuk a háziorvosnál
To confirm the quality of a product, GMP regulations are strictly followed. It is a standard policy with basic rules or guidelines that are followed by numerous companies to prove the quality of their
Expert witness view of fda regulated companies - information trial attorneys ...Joshua Sharlin, Ph.D.
1. Learn an expert witness’s view about common problems and errors in the processes FDA requires
2. Understand how information is collected and reported in today’s FDA-regulated environment
3. Identify documents that add to a knowledgebase about the activities and results of FDA-regulated processes
Acid Indigestion / Heartburn/ Pyrosis Global Clinical Trials Review, H1, 2013
Summary
GlobalData's clinical trial report, 'Acid Indigestion / Heartburn/ Pyrosis Global Clinical Trials Review, H1, 2013" provides data on the Acid Indigestion / Heartburn/ Pyrosis clinical trial scenario. This report provides elemental information and data relating to the clinical trials on Acid Indigestion / Heartburn/ Pyrosis. It includes an overview of the trial numbers and their recruitment status as per the site of trial conduction across the globe. The databook offers a preliminary coverage of disease clinical trials by their phase, trial status, prominence of the sponsors and also provides briefing pertaining to the number of trials for the key drugs for treating Acid Indigestion / Heartburn/ Pyrosis. This report is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GlobalData's team of industry experts.Note: Certain sections in the report may be removed or altered based on the availability and relevance of data for the indicated disease.
Scope
- Data on the number of clinical trials conducted in North America, South and Central America, Europe, Middle-East and Africa and Asia-pacific and top five national contributions in each, along with the clinical trial scenario in BRIC nations - Clinical trial (complete and in progress) data by phase, trial status, subjects recruited and sponsor type- Listings of discontinued trials (suspended, withdrawn and terminated)
Reasons to buy
- Understand the dynamics of a particular indication in a condensed manner- Abridged view of the performance of the trials in terms of their status, recruitment, location, sponsor type and many more- Obtain discontinued trial listing for trials across the globe- Espy the commercial landscape of the major Universities / Institutes / Hospitals or Companies
Satisfying us and eu human factors requirements for inhaler devicesCambridge Consultants
HFE is an essential and integral part of the inhaler device development process. The process requirements are primarily based on the core principles of safety and effectiveness. The HFE processes for the FDA and EU submissions are largely harmonized, but there are some minor differences. It is important that manufacturers of inhaler devices understand the process clearly so that they can comply with the requirements. Following the HFE process does not only fulfil the regulatory requirements but also helps you to develop better products. This presentation provides the holistic view of the HFE process in a simple schematic way, however every project is different and the process should be tailored accordingly.
Making PrescriptionsPpersonal - Pharmacogenomics reports - Software in MedicineGDG Budapest
10 éven belül valóra válhatna az a még
kissé futurisztikusnak tűnő kép, hogy mindenkiről egy genetikai
polimorfizmus adattár áll rendelkezésre mondjuk a háziorvosnál
To confirm the quality of a product, GMP regulations are strictly followed. It is a standard policy with basic rules or guidelines that are followed by numerous companies to prove the quality of their
Integra gen s.a (alint) product pipeline analysis, 2014 updateAmbikabasa
Summary IntegraGen S.A (IntegraGen) is a biotechnology service provider. The company provides clinical genomic services to academic researchers and life sciences companies. It offers services such as DNA extraction, management samples, study design, strategy, selection markers, tagging, biostatistics analysis, and bioinformatics analysis of sequence data. IntegraGen provides sequencing and genotyping of DNA and RNA. The company offers services in the fields of pharmacogenetics, cytogenetics, epigenetics, and agriculture. It serves patients, clinicians and researchers. IntegraGen partners with illumia, Fluidigm, DNA genotek and Agitent Certified companies.
http://www.researchmoz.us/integragen-sa-alint-product-pipeline-analysis-2014-update-report.html
Therapure biopharma inc. product pipeline review - 2015Ambikabasa
This report provides comprehensive information on the current therapeutic developmental pipeline of Therapure Biopharma Inc.s, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/therapure-biopharma-inc-product-pipeline-review-2015-report.html
This report provides comprehensive information on the current therapeutic developmental pipeline of Genzyme Corporations, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/genzyme-corporation-product-pipeline-review-2015-report.html
Co mentis, inc. product pipeline review - 2015Ambikabasa
This report provides comprehensive information on the current therapeutic developmental pipeline of CoMentis, Inc.s, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/comentis-inc-product-pipeline-review-2015-report.html
Myriad genetics, inc. product pipeline analysisraja1233
Companyprofilesandconferences.com glad to promote a new report on "Myriad Genetics, Inc. (MYGN) - Product Pipeline Analysis" which is a source for data, analysis, and actionable intelligence on the company’s portfolio of pipeline products who provides key information about the company, its major products and brands.
Market Research Reports, Inc. has announced the addition of “Acute Lung Injury - Pipeline Insight, 2018” research report to their offering. See more at - http://mrr.cm/Unn
Arrhythmias - Pipeline Review, H1 2015 Summary Global Markets Directs, Arrhythmias - Pipeline Review, H1 2015, provides an overview of the Arrhythmiass therapeutic pipeline. This report provides comprehensive information on the therapeutic development for Arrhythmias, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Arrhythmias and special features on late-stage and discontinued projects.
http://www.researchmoz.us/arrhythmias-pipeline-review-h1-2015-report.html
Quantum genomics sa product pipeline review - 2015Ambikabasa
This report provides comprehensive information on the current therapeutic developmental pipeline of Quantum Genomics SAs, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/quantum-genomics-sa-product-pipeline-review-2015-report.html
Integra gen s.a (alint) product pipeline analysis, 2014 updateAmbikabasa
Summary IntegraGen S.A (IntegraGen) is a biotechnology service provider. The company provides clinical genomic services to academic researchers and life sciences companies. It offers services such as DNA extraction, management samples, study design, strategy, selection markers, tagging, biostatistics analysis, and bioinformatics analysis of sequence data. IntegraGen provides sequencing and genotyping of DNA and RNA. The company offers services in the fields of pharmacogenetics, cytogenetics, epigenetics, and agriculture. It serves patients, clinicians and researchers. IntegraGen partners with illumia, Fluidigm, DNA genotek and Agitent Certified companies.
http://www.researchmoz.us/integragen-sa-alint-product-pipeline-analysis-2014-update-report.html
Therapure biopharma inc. product pipeline review - 2015Ambikabasa
This report provides comprehensive information on the current therapeutic developmental pipeline of Therapure Biopharma Inc.s, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/therapure-biopharma-inc-product-pipeline-review-2015-report.html
This report provides comprehensive information on the current therapeutic developmental pipeline of Genzyme Corporations, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/genzyme-corporation-product-pipeline-review-2015-report.html
Co mentis, inc. product pipeline review - 2015Ambikabasa
This report provides comprehensive information on the current therapeutic developmental pipeline of CoMentis, Inc.s, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/comentis-inc-product-pipeline-review-2015-report.html
Myriad genetics, inc. product pipeline analysisraja1233
Companyprofilesandconferences.com glad to promote a new report on "Myriad Genetics, Inc. (MYGN) - Product Pipeline Analysis" which is a source for data, analysis, and actionable intelligence on the company’s portfolio of pipeline products who provides key information about the company, its major products and brands.
Market Research Reports, Inc. has announced the addition of “Acute Lung Injury - Pipeline Insight, 2018” research report to their offering. See more at - http://mrr.cm/Unn
Arrhythmias - Pipeline Review, H1 2015 Summary Global Markets Directs, Arrhythmias - Pipeline Review, H1 2015, provides an overview of the Arrhythmiass therapeutic pipeline. This report provides comprehensive information on the therapeutic development for Arrhythmias, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Arrhythmias and special features on late-stage and discontinued projects.
http://www.researchmoz.us/arrhythmias-pipeline-review-h1-2015-report.html
Quantum genomics sa product pipeline review - 2015Ambikabasa
This report provides comprehensive information on the current therapeutic developmental pipeline of Quantum Genomics SAs, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/quantum-genomics-sa-product-pipeline-review-2015-report.html
1. AnaZyme, LLC - Product Pipeline Analysis
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2. AnaZyme, LLC - Product Pipeline Analysis
Summary
AnaZyme, LLC, (AnaZyme) is a diagnostic assay company. The company was established in collaboration with
researchers from the Bioengineering Department at UC San Diego. It was created as a direct result from the
research and development of InfammaGen, a new therapy that reduces morbidity and mortality related to multi-
organ failure and death as a result of acute shock. Researchers have discovered various biomarkers to diagnose
the onset of shock and its progression during treatment. Three assays have been created from these biomarkers in
both animal and human samples. The three assays include exhaled breath-based assay to detect volatile
compounds; blood-based assay to detect specific enzymes and blood-based assay to detect the absence of
specific compounds. These assays can be run on commercially available general purpose laboratory instruments
and current hospital testing devices. AnaZyme is headquartered in San Diego, California, the US.
This report is a source for data, analysis and actionable intelligence on the AnaZyme, LLC portfolio of pipeline products.
The report provides detailed analysis on each pipeline product with information on the indication, the development
stage, trial phase, product milestones, pipeline territory, estimated approval date, and estimated launch date
Each pipeline product is profiled to cover information on product description, function, technology, indication, and
application. The report is also supplemented with a detailed company profile and information on clinical trials,
wherever applicable.
This report is built using data and information sourced from proprietary databases, primary and secondary research and
in-house analysis by GlobalData’s team of industry experts.
3. Scope
- Detailed company profile with information on business description, key company facts, major products and
services, key competitors, key employees, locations and subsidiaries and recent developments.
- Detailed coverage on all the pipeline products, by equipment type, by therapy area, by development stage, and
by trial phase.
- Information on product milestones and pipeline territory for each product, the estimated approval date, and
estimated launch date.
- Profile of each pipeline product with additional information on product description, function, technology,
indication(s), and application.
- Data on relevant clinical trials and product patent details, wherever applicable.
- Information on clinical trial, wherever applicable, is supplemented with information on trial phase, trial status,
trial objective, trial design, target patients, unique physician identifier, primary point, secondary point, acronym,
participants inclusion, participants exclusion, interventions, trial results, trial start date, trial end date, study
type, trial site, trial funding, age eligibility, and gender eligibility.
4. Reasons to Buy
- Develop business strategies by understanding the trends and developments driving the medical devices
pipeline and technology landscape globally.
- Design and develop your product development, marketing and sales strategies.
- Exploit M&A opportunities by identifying market players with the most innovative pipeline.
- Develop market-entry and market expansion strategies.
- Exploit in-licensing and out-licensing opportunities by identifying products, most likely to ensure a robust
return.
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to
gain competitive advantage.
- Develop competition strategies by identifying the status and likely launch of your competitors’ pipeline
products through review of the clinical trials, stage and phase of development, etc.- Which are the next high-
value products that your competitor would add in its portfolio? – identify, understand and capitalize.
5. List of Tables 3
List of Figures 3
Key Facts 4
AnaZyme, LLC - Major Products and Services 5
AnaZyme, LLC Pipeline Products by Equipment Type 6
AnaZyme, LLC Pipeline Products by Development Stage 8
AnaZyme, LLC Pipeline Products by Therapy Area 10
AnaZyme Blood Assay – Absence Of Specific Compounds 12
AnaZyme Blood Assay – Absence Of Specific Compounds Product Status 12
AnaZyme Blood Assay – Absence Of Specific Compounds Product Description 12
AnaZyme Blood Assay – Absence Of Specific Compounds Product Patent Details 12
AnaZyme Blood Assay – Specific Enzymes 14
AnaZyme Blood Assay – Specific Enzymes Product Status 14
AnaZyme Blood Assay – Specific Enzymes Product Description 14
AnaZyme Blood Assay – Specific Enzymes Product Patent Details 14
AnaZyme Breath Assay – Volatile Com-pounds 16
AnaZyme Breath Assay – Volatile Com-pounds Product Status 16
AnaZyme Breath Assay – Volatile Com-pounds Product Description 16
AnaZyme Breath Assay – Volatile Com-pounds Product Patent Details 16
AnaZyme, LLC - Key Competitors 18
AnaZyme, LLC - Key Employees 19
AnaZyme, LLC - Locations And Subsidiaries 20
Head Office 20
Appendix 21
Methodology 21
About GlobalData 21
Contact Us 21
Disclaimer 21
6. List of Tables
AnaZyme, LLC, Key Facts 1
AnaZyme, LLC Key Pipeline Products by Equipment Type 1
AnaZyme, LLC Key Pipeline Products by Therapy Area 1
AnaZyme, LLC Key Pipeline Products by Development Stage 1
AnaZyme, LLC, Key Facts 4
AnaZyme, LLC, Major Products and Services 5
AnaZyme, LLC Number of Pipeline Products by Equipment Type 6
AnaZyme, LLC Pipeline Products by Equipment Type 7
AnaZyme, LLC Number of Pipeline Products by Development Stage 8
AnaZyme, LLC Pipeline Products by Development Stage 9
AnaZyme, LLC Number of Pipeline Products by Therapy Area 10
AnaZyme, LLC Pipeline Products by Therapy Area 11
AnaZyme Blood Assay – Absence Of Specific Compounds - Product Status 12
AnaZyme Blood Assay – Absence Of Specific Compounds - Product Description 12
AnaZyme Blood Assay – Absence Of Specific Compounds - Patent Details1 12
AnaZyme Blood Assay – Absence Of Specific Compounds - Patent Details2 13
AnaZyme Blood Assay – Specific Enzymes - Product Status 14
AnaZyme Blood Assay – Specific Enzymes - Product Description 14
AnaZyme Blood Assay – Specific Enzymes - Patent Details1 14
AnaZyme Blood Assay – Specific Enzymes - Patent Details2 15
AnaZyme Breath Assay – Volatile Com-pounds - Product Status 16
AnaZyme Breath Assay – Volatile Com-pounds - Product Description 16
AnaZyme Breath Assay – Volatile Com-pounds - Patent Details1 16
AnaZyme Breath Assay – Volatile Com-pounds - Patent Details2 17
AnaZyme, LLC, Key Employees 19
7. List of Figures
AnaZyme, LLC Pipeline Products by Equipment Type 6
AnaZyme, LLC Pipeline Products by Development Stage 8
AnaZyme, LLC Pipeline Products by Therapy Area 10
8. Related Reports
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