Toscana Biomarkers Srl - Product Pipeline Analysis, 2013 Update - New Study Released

From: Fast Market Research, Inc.
Published: Fri Nov 15 2013

Toscana Biomarkers Srl (Toscana) is a biotechnological research and development service provider. The company develops and validates innovative test in the field of autoimmune disease diagnosis. Its products include biomarkers and diagnostic tests. Toscana's Biomarkers are decision-making tools on basis of clinical diagnostics used for therapeutic treatments. The company's in-vitro tests are based on the detection of antibodies as disease biomarkers used for the diagnosis and the follow-up of autoimmune disorders. The company provides in vitro tests such as autoantibody blood tests, blood tests to measure inflammation and organ function, clinical presentation and MRI examinations. Toscana is headquartered in Siena, Toscana, Italy.

This report is a source for data, analysis and actionable intelligence on the Toscana Biomarkers Srl 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

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.


* 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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