GenMark Diagnostics, Inc. (GNMK) - Product Pipeline Analysis || Aarkstore Enterprise

Nov. 23, 2011 - PRLog -- http://www.aarkstore.com/reports/GenMark-Diagnostics-Inc-GNMK-Product-Pipeline-Analysis-164256.html

Summary

GenMark Diagnostics, Inc.is engaged in the manufacturing, development, design and distribution of molecular diagnostic technologies and tools. The flagship product of the company is eSensor XT-8 System. The XT8 system provides Warfarin Sensitivity Test, Thrombophilia Risk Test, Respiratory Viral Panel Test and Cystic Fibrosis Genotyping Test. The company also developing diagnostic tests for an individual’s sensitivity to Plavix. The pipeline product of the company includes NexGen system (formerly referred to as the AD-8 system), K-ras Mutation, Oncology and Personalized Medicine Tests It principally operates in the US. The company is headquartered in California, US.

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