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  • Please comment on the clinical need of your diagnostic assay. (For example, how the diagnostic assay will improve healthcare). Maximum 100 words.
  • What is the biological rationale that detection of the target analyte can lead to an improved clinical outcome? Please include supporting peer reviewed publications, including your own.
  • Describe the technology readiness of your diagnostic assay. Include a brief description of the assay, associated technology and reagents. (For example, describe if you have a working assay and how much testing has been carried out to date). Maximum 200 words.
  • What published literature is there on the diagnostic target or its clinical utility? This may include your published data and other pertinent citations. Maximum 100 words.
  • Comment on what reagents you currently have available or could be readily produced. (For example, peptides, proteins, antibodies, RNA, DNA, standards or controls). Maximum 150 words.
  • Provide details of the level of resources committed to the project to date including the number of staff currently working on the project. Maximum 100 words.
  • Do you have any IP in the area and is there any competing IP/research? Briefly detail and if appropriate give patent number(s), priority date(s) and status. Maximum 100 words.
  • What is the current status and next stage of the project? How will a collaboration with LifeArc support the development of the project? Maximum 200 words.
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