New Medical Devices research report from GlobalData is now available from Fast Market Research
Boston, MA -- (SBWIRE) -- 08/01/2012 -- Simbex is a medical device company, based in the US. It conducts research and develops biomechanical feedback systems. The company provides activestep, head impact telemetry system include riddell SRS and riddell IQ HITS, and active contact. Its activestep is a mobility simulator that replicates real-world bumps, trips, and slips that often result in a fall to more quickly and effectively sharpen the step-recovery reflex to prevent falls. The company's head impact telemetry system is commercially available system that can measure head accelerations in real-time during games and practices. It maintains a robust technology development and systems integration capacity - the core competence is biomechanics. Simbex is headquartered in Lebanon, New Hampshire, the US.
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This report is a source for data, analysis and actionable intelligence on the Simbex 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.
- 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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