Boston, MA -- (ReleaseWire) -- 11/26/2013 -- HEPQUANT, LLC (HEPQUANT) is a medical device company. The company develops and markets products for measuring liver function. HEPQUANT's products include HepQuant-STAT, HepQuant-SHUNT, and HepQuant-FLOW. Its HepQuant-STAT is used in screening assay to identify patients with diminished liver function due to undiagnosed chronic liver disease; HepQuant-SHUNT is designed to assess the portal circulation; and HepQuant-FLOW is developed to assess portal blood flow. The company's products improve diagnosis and aid clinical management. HEPQUANT provides analysis and assessments of research applications of hepquant tests; pocessing and analysis of serum samples; and analysis of data and relationship to utility and outcomes. It serves patients suffering from chronic liver disease. HEPQUANT is headquarterd in Greenwood Village, Colorado, the US.
This report is a source for data, analysis and actionable intelligence on the HEPQUANT, 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.
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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.
- 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.
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