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COAGULATION-LIMITED, VALIDATED MAT'L - CGM
CGM
Analytes/procedures in bold type are regulated for proficiency testing by the Centers for Medicare & Medicaid Services (CMS).

Analyte Challenges per Shipment Number of Shipments
Activated partial thromboplastin time 5 See Samples tab below
Fibrinogen 5
International normalized ratio (INR) 5
Prothrombin time 5
D-dimer 2
Fibrin(ogen) degradation products, plasma 1
Fibrin(ogen) degradation products, serum 1

Improve the reliability of your patient results with CAP Survey Validated Materials

Use the same material that is sent in the Surveys program to:

  • Identify and troubleshoot instrument / method problems
  • Correlate results with other laboratories or instruments
  • Document correlation of problems identified in Surveys
  • Utilize material with confirmed results as an alternative external quality control
  • Identify potential proficiency testing failures
Each laboratory receives a Survey Participant Summary, which includes readily available results


Program Information

  • Five 1.0‑mL lyophilized plasma specimens; three shipments per year
  • One 1.0‑mL plasma specimen and one 1.0-mL serum specimen; two shipments per year

Shipping Schedule

  • Shipment A: January 24
  • Shipment B: May 9
  • Shipment C: August 22






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