Boston, MA -- (SBWIRE) -- 02/25/2014 -- PositiveID Corporation (PositiveID) is a medical device manufacturer. The company develops microfluidic systems for automated preparation and performance of biological assays. It detects biological threats for homeland defense as well as analyzes biological samples at the point of care. The company provides molecular diagnostic and diabetes management products. PositiveID's molecular diagnostic products include M-BAND, DragonFlya and Firefly. It develops complex microfluidic systems to perform sample processing and purification for the Defense Advanced Projects Agency. The companys diabetes management division is focused on an in-vivo continuous blood glucose monitoring and non-invasive breath glucose detection device that is designed to measure exhaled acetone levels. PositiveID is headquartered in Delray Beach, Florida, the US.

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This report is a source for data, analysis and actionable intelligence on the PositiveID Corporation 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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