Boston, MA -- (SBWIRE) -- 07/18/2012 -- AutoGenomics, Inc. (AutoGenomics) is a manufacturer of automated and integrated solution, based in the US. The company designs, develops, manufactures and markets molecular diagnostic products for the in-vitro diagnostic markets. Its products include INFINITI system which automates the discrete processes of genetic testing performed by clinical laboratories. INFINITI system consists of the INFINITI Analyzer and the consumable products used to run tests on its system, including the BioFilmChip Microarray and the Intellipac Reagent Management Module. The company's products are used in the fields of genetic disorders, cancer, infectious diseases and pharmacogenetics. It is partnered with American International Biotechnology Services. The company products are certified with ISO 13485 for its quality management systems. AutoGenomics is headquartered in Vista, California, the US.

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