NanoSpeed Diagnostics Inc. (NanoSpeed) is a diagnostics services provider. It carries out the development of proprietary diagnostic/screening test kit platforms based on lateral flow immunoassay and our Lab-On-a-Chip (LOC) technology. The company’s products cater to the needs of the healthcare industry, regulatory agencies and consumers. It carries out research and development in the field of antibiotics, vitamin d total, cancer biomarkers and pathogens. NanoSpeed is headquartered in Edmonton, Alberta, Canada. Nanospeed Diagnostics Inc. aims to be a recognized global leader focused on providing portable, innovative and rapid testing solutions for healthcare, food safety, and agricultural industry sectors. To this end, the company introduced Test4D POC test at the WAVE 2011 Conference in Lake Louise and Health Technology Symposium in Edmonton.
This report is a source for data, analysis and actionable intelligence on the NanoSpeed 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.
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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