Report Published: "Seegene, Inc. (096530) - Product Pipeline Analysis, 2013 Update"

Seegene, Inc. (Seegene) is a molecular diagnostic company. The company specializes in molecular diagnostics and develops technology and products. Its products include magicplex, anyplex, seeplex, and instuments among others. The company's research and development wing concentrates on developing new technologies and products to the healthcare markets. Seegene also provides genome diagnostic kits for research purposes. Seegene analyzes genes to determine the existence of disease through an in vitro diagnostic tool molecular diagnostic. It provides conventional methods such as incubation diagnostics and immunodiagnosis. The company's products are used in testing for infectious diseases such as respiratory virus and sexually transmitted diseases. Seegene is headquartered in Seoul, Korea.

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

Full Report Details at
- http://www.fastmr.com/prod/723206_seegene_inc_096530_product_pipeline_analysis_2013.aspx?afid=301

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.

Reasons to Get this Report

* Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.

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