"Thornhill Research Inc - Product Pipeline Analysis, 2013 Update" Published

Thornhill Research Inc (Thornhill) is a medical device company. The company develops and manufactures medical devices for cardiovascular diagnostics, neuro imaging, EMS/Field medicine, and drug safety. Its products include MOVES, RespirAct, ClearMate and PAXLight. MOVES is a life support system, which maintains delivered oxygen concentrations for ventilated patients. Thornhill's RespirAct gas flow controller is a device that is designed to control end-tidal gas concentrations in the lungs and blood. The company's ClearMate is a gas washout system that is designed to eliminate hydrocarbons from the lung. PAXLight is a LED field hospital light. It also provides research and development facility. The company is ISO 13485:2003 certified. Thornhill is headquartered in Toronto, Ontario, Canada.

Full Report Details at
- http://www.fastmr.com/prod/643519_thornhill_research_inc_product_pipeline_analysis.aspx?afid=301

This report is a source for data, analysis and actionable intelligence on the Thornhill Research 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.

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.

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.

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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