New Medical Devices research report from GlobalData is now available from Fast Market Research
Boston, MA -- (SBWIRE) -- 07/18/2012 -- Medisse BV (Medisse) is a biotechnology company that carries out the development of resorbable medical implants for soft tissue applications. It offers products such as FlexiSurge Mesh bio-resorbable film and FlexiSurge adhesion barrier, which are based on a material formed from PTMC (Poly 1, 3- trimethylene carbonate) networks. The company's products find application in gynecology, general surgery, dermatology, drug delivery and ophthalmology. Its products comprises staple-line reinforcement products and periodontal sheets. The company has its own proprietary technology for making PTMC networks and its laboratory is located in the premises of the University of Twente.
This report is a source for data, analysis and actionable intelligence on the Medisse BV 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.
View Full Report Details and Table of Contents
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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