Boston, MA -- (SBWIRE) -- 02/21/2013 -- Harbor MedTech, Inc. (Harbor) develops and commercializes wound healing technology. Harbor has strategic partnership with Edwards Lifesciences, a xenograft-based device company, in which the company acquired the exclusive license of patented collagen stabilizing technology, BriDGE. Extensive studies carried out by Edwards and other independent researchers have shown that BriDGE processed xenografts support fast healing and an unprecedented degree of control over the softness, strength, and resorbability of its products. The company is commercializing a portfolio of products with its BriDGE technology platform. Its first product Architect ECM, a wound therapy for chronic wounds such as diabetic, venous and pressure ulcers. Other products in development stage include advanced solutions for joint repair, hernia repair, breast reconstruction, and urogynecological repair. Harbor is headquartered in Irvine, California, the US.

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This report is a source for data, analysis and actionable intelligence on the Harbor MedTech, 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.

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