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PARALLAX DIAGNOSTICS, INC.
|
10-Q
Aug 11, 4:58 PM ET
PARALLAX DIAGNOSTICS, INC. 10-Q
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Contents
7
1. is or becomes publicly available (other than through unauthorized disclosure under this Agreement);
2. is already known by the Supplier without an obligation of confidentiality prior to the disclosure thereof by PRLX, as evidenced by the Supplier's written records, maintained in the ordinary course, existing before the first date of Supplier's engagement with PRLX; or
3. is rightfully received by the Supplier from a third party free of any obligation of confidentiality.
Statement of Work
Supplier will manufacture assays and supply a Data Package for Parallax. The Data Package will include all existing Standard Operating Proceedures (SOP’s) related to the manufacture of the Target assays as well as new SOP’s that Supplier will create in order to manufacture Target assays. New SOP’s will include a flow chart detailing the procurement and manufacture of assays, a supplier list, methods for manufacture, quality control procedures and any other documents or procedures necessary for the manufacture of Target Assays.
Based on raw material availability and manufacturing time this quote is based on one or a combination of the CRP assay, HCG assay and/or Rotavirus assay. The cost below will yield approximately 100 to 200 fully functional assay test devices for internal investigational use. Estimated delivery of the assays is eight (8) weeks from the Effective Date of this Agreement.
Material Qualification/Reagent & Membrane Processing/Quality Control (76 hours) Device Assembly/Reagent Filling/Packaging (20 hours)