New Medical Devices market report from GlobalData: "Phthisis Diagnostics, Inc. - Product Pipeline Analysis"
Boston, MA -- (SBWIRE) -- 02/25/2013 -- Phthisis Diagnostics, Inc. (Phthisis Diagnostics) is a biotechnology company. The company's product portfolio comprises E-Sphere Simple NA Kit for extraction of nucleic acids from samples; and G-Sphere molecular standard. It is developing E-Sphere simple DNA kit to extract DNA from clinical samples; R-Sphere CG detect to identify giardia and cryptosporidium from stool samples; and R-Sphere microsporidia detect. Phthisis Diagnostics collaborates with clinical diagnostic labs, biotechnology companies and public health labs to develop molecular diagnostic tests. Through different distributors, the company distributed its products to various international markets including Canada, India, Taiwan, Belgium, and the UK among others. Phthisis Diagnostics is headquartered in Charlottesville, Virginia, the US.
This report is a source for data, analysis and actionable intelligence on the Phthisis Diagnostics, Inc. 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.
Reasons to Get this Report
- Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.
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