Saturday, 30 June 2012

Cytograft Tissue Engineering - Product Pipeline Analysis

Cytograft Tissue Engineering, Inc. (CTE) is a medical device company, based in the US. The company develops cell-based solutions to cardiovascular disease. Its product line includes TEBV (Tissue Engineered Blood Vessel), covered stent, patch, percutaneous bypass and valve. CTE’s follow-on products include the LifeGuar patch and the LifeJacket stent-graft. LifeLine is a versatile technology that has the potential to be used for coronary bypass, as a peripheral graft for the prevention of lower limb amputation, or as an arterio-venous shunt for hemodialysis access. It has collaborations with physicians and scientists from Stanford University, the University of Washington, the Minneapolis Heart Institute, the Hope Heart Institute, and the University of Missouri. CTE is headquartered in Novato, California, the US.

This report is a source for data, analysis and actionable intelligence on the Cytograft Tissue Engineering, 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.

Scope

- Detailed Cytograft Tissue Engineering 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 Cytograft Tissue Engineering 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 Cytograft Tissue Engineering 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 Buy

- Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.
- Design and develop your product development, marketing and sales strategies.
- Exploit M&A opportunities by identifying market players with the most innovative pipeline.
- Develop market-entry and market expansion strategies.
- Exploit in-licensing and out-licensing opportunities by identifying products, most likely to ensure a robust return.
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
- Develop competition strategies by identifying the status and likely launch of your competitors’ pipeline products through review of the clinical trials, stage and phase of development, etc.
- Which are the next high-value products that your competitor would add in its portfolio? – identify, understand and capitalize.

To view the detailed table of contents for this report please visit: http://www.reportstack.com/product/84709/cytograft-tissue-engineering-inc-product-pipeline-analysis.html

ValveXchange - Product Pipeline Analysis

ValveXchange, Inc. (ValveXchange) is a medical device company, based in the US. It develops medical products for cardiovascular markets. The company develops two-part bioprosthetic tissue valves using its patented VXi technology. Its products include surgically implantable valve, transapically implantable valve, exchange tool set, and apical introducer. ValveXchange’s valve exchange procedure can be used in open surgeries, invasive surgical procedures and transcatheter depending on the clinical indication of the patient and physician experience. It has entered in to an option agreement with Dr. Gerard Guiraudon to license his Universal Cardiac Introducer technology. The products offered by the company are approved by FDA. The company has received an equity investment of $3.5m from CryoLife Inc., a tissue processing and medical device company focused on cardiac and vascular surgery. ValveXchange is headquartered in Greenwood Village, Colorado, the US.

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

Scope

- Detailed ValveXchange 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 ValveXchange 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 ValveXchange 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 Buy

- Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.
- Design and develop your product development, marketing and sales strategies.
- Exploit M&A opportunities by identifying market players with the most innovative pipeline.
- Develop market-entry and market expansion strategies.
- Exploit in-licensing and out-licensing opportunities by identifying products, most likely to ensure a robust return.
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
- Develop competition strategies by identifying the status and likely launch of your competitors’ pipeline products through review of the clinical trials, stage and phase of development, etc.
- Which are the next high-value products that your competitor would add in its portfolio? – identify, understand and capitalize.

To view the detailed table of contents for this report please visit: http://www.reportstack.com/product/84707/valvexchange-inc-product-pipeline-analysis.html

Orthox Ltd. - Product Pipeline Analysis

Orthox Ltd (Orthox) is a medical device company, based in the UK. It develops products to regenerate damaged cartilage and bone tissues. The company’s products include FibroFix Meniscus and FibroFix Cartilage. The product FibroFix Meniscus is designed to repair and regenerate the tough, shock absorbing meniscal cartilage in the knee and it replaces the tissue removed in a meniscectomy procedure. Its FibroFix Cartilage is developed to treat the damage done to the articular cartilage in the knee and it enables the surgeon to resurface the articular cartilage defect in the earlier stage. The company markets its products through its brands, FibroFix Meniscus and FibroFix Cartilage. It operates as a subsidiary of Oxford Biomaterials. Orthox is headquartered in Oxfordshire, the UK.

This report is a source for data, analysis and actionable intelligence on the Orthox 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 Orthox 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 Orthox 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 Orthox pipeline product with additional information on product description, function, technology, indication(s), and application.
- Data on relevant Orthox clinical trials and product patent details, wherever applicable.
- Information on Orthox 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 Buy

- Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.
- Design and develop your product development, marketing and sales strategies.
- Exploit M&A opportunities by identifying market players with the most innovative pipeline.
- Develop market-entry and market expansion strategies.
- Exploit in-licensing and out-licensing opportunities by identifying products, most likely to ensure a robust return.
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
- Develop competition strategies by identifying the status and likely launch of your competitors’ pipeline products through review of the clinical trials, stage and phase of development, etc.
- Which are the next high-value products that your competitor would add in its portfolio? – identify, understand and capitalize.

To view the detailed table of contents for this report please visit: http://www.reportstack.com/product/84705/orthox-ltd-product-pipeline-analysis.html

Jemo Spine - Product Pipeline Analysis

Jemo Spine, LLC. (Jemo Spine) is a privately-held medical device company, based in the US. It designs, develops, manufactures and markets orthopedic products for the spine market. The company designs and develops spinal fusion and fixation systems used by the orthopedic surgeons during minimally invasive surgical procedures. Its product portfolio includes classic fusion, dynamic and biologics. Jemo Spine’s classic fusion products are delta, alta and moab. Its dynamic products include smartu, s-flex, spinoflex, spinofix, omega and moab. The company’s biologics consists of BTCP product. Its surgical instruments are made with a stainless steel. The company is ISO 7153/1 certified. Jemo Spine is headquartered in Murray, Utah, the US.

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

Scope

- Detailed Jemo Spine 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 Jemo Spine 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 Jemo Spine 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 Buy

- Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.
- Design and develop your product development, marketing and sales strategies.
- Exploit M&A opportunities by identifying market players with the most innovative pipeline.
- Develop market-entry and market expansion strategies.
- Exploit in-licensing and out-licensing opportunities by identifying products, most likely to ensure a robust return.
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
- Develop competition strategies by identifying the status and likely launch of your competitors’ pipeline products through review of the clinical trials, stage and phase of development, etc.
- Which are the next high-value products that your competitor would add in its portfolio? – identify, understand and capitalize.

To view the detailed table of contents for this report please visit: http://www.reportstack.com/product/84703/jemo-spine-llc-product-pipeline-analysis.html

Palmaz Scientific - Product Pipeline Analysis

Palmaz Scientific, Inc. (Palmaz) is a medical technology company, based in the US. It research and develops novel technologies in the field of interventional cardiology. The company markets its product through its brand name Palmaz Stent. Palmaz product Palmaz Stent is an expandable intravascular stent that has been created safe, more predictable implantable prosthetic devices, which improve the patient outcomes and quality of life. It conducts research and development operations in Fremont, California. The company has a strong intellectual property portfolio of patented and patent pending thin film metal surface technologies and processing methods. Palmaz is headquartered in Dallas, Texas, the US.

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

Scope

- Detailed Palmaz Scientific 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 Palmaz Scientific 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 Palmaz Scientific 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 Buy

- Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.
- Design and develop your product development, marketing and sales strategies.
- Exploit M&A opportunities by identifying market players with the most innovative pipeline.
- Develop market-entry and market expansion strategies.
- Exploit in-licensing and out-licensing opportunities by identifying products, most likely to ensure a robust return.
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
- Develop competition strategies by identifying the status and likely launch of your competitors’ pipeline products through review of the clinical trials, stage and phase of development, etc.
- Which are the next high-value products that your competitor would add in its portfolio? – identify, understand and capitalize.

To view the detailed table of contents for this report please visit: http://www.reportstack.com/product/84702/palmaz-scientific-inc-product-pipeline-analysis.html

Corentec Co - Product Pipeline Analysis

Corentec Co., Ltd. (Corentec) is a medical equipment company, based in Korea. The company develops and manufactures artificial joints and spinal implant solutions. The company’s products include spinal, hip, knee and the bone substitutes. It offers spine products such as, saddle mounted onto pedicle screws; sleeves to prevent the head from opening wider and bone substitutes include BDP granule, block, porous metal, and TZP or HA products. The company’s knee products include wide range of fixed and mobile bearings. It is certified with ISO 9001:2000 and ISO 13485:2003 for its quality management systems. Corentec is headquartered in Seoul, Korea.

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

Scope

- Detailed Corentec 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 Corentec 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 Corentec 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 Buy

- Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.
- Design and develop your product development, marketing and sales strategies.
- Exploit M&A opportunities by identifying market players with the most innovative pipeline.
- Develop market-entry and market expansion strategies.
- Exploit in-licensing and out-licensing opportunities by identifying products, most likely to ensure a robust return.
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
- Develop competition strategies by identifying the status and likely launch of your competitors’ pipeline products through review of the clinical trials, stage and phase of development, etc.
- Which are the next high-value products that your competitor would add in its portfolio? – identify, understand and capitalize.

To view the detailed table of contents for this report please visit: http://www.reportstack.com/product/84700/corentec-co-ltd-product-pipeline-analysis.html

Akonni Biosystems - Product Pipeline Analysis

Akonni Biosystems Inc (Akonni Biosystems) is a diagnostics company based in the US. The company develops, manufactures, and markets integrated molecular diagnostic systems. It provides products for markets such as, clinical and life science research markets. The products of the company include, nucleic acid extraction kits, MDx tests and instruments and software. Akonni trudiagnosis systems of Akonni Biosystems which is provided for clinical markets enables rapid and affordable testing for a variety of molecular markers associated with human diseases on a gel-drop microarray platform. Akonni TruTip Kits provided for life science research markets provides life science research and molecular laboratories with an affordable, rapid and robust means of extracting nucleic acids. Akonni Biosystems is headquartered in Frederick, Maryland, the US.

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

Scope

- Detailed Akonni Biosystems 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 Akonni Biosystems 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 Akonni Biosystems 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 Buy

- Develop business strategies by understanding the trends and developments driving the medical devices pipeline and technology landscape globally.
- Design and develop your product development, marketing and sales strategies.
- Exploit M&A opportunities by identifying market players with the most innovative pipeline.
- Develop market-entry and market expansion strategies.
- Exploit in-licensing and out-licensing opportunities by identifying products, most likely to ensure a robust return.
- Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage.
- Develop competition strategies by identifying the status and likely launch of your competitors’ pipeline products through review of the clinical trials, stage and phase of development, etc.
- Which are the next high-value products that your competitor would add in its portfolio? – identify, understand and capitalize.

To view the detailed table of contents for this report please visit: http://www.reportstack.com/product/84696/akonni-biosystems-inc-product-pipeline-analysis.html