Crystal Digital PCR™ Operational Qualification (OQ) Solutions Taking digital PCR to the next level with Crystal Digital PCR™ technology Stilla Technologies’ Crystal Digital PCR™ technology for absolute quantification of nucleic acids is based on cutting-edge microfluidic technology that integrates the digital PCR process in a single consumable, reducing hands-on time and interaction. Crystal Digital PCR™ technology provides the complete workflow for digital PCR and is designed to provide a sensitive, robust, fast, and easy-to-use solution. Importance of routine qualification of Crystal Digital PCR™ systems to exploit the full potential of Crystal Digital PCR™ Any Crystal Digital PCR™ system installation starts with a full Installation Qualification (IQ) and Operational Qualification (OQ) performed by a qualified Stilla Technologies expert to ensure optimal conditions for the precise and highly sensitive dPCR quantification. Routine OQ verifies that laboratory instruments meet specified operating criteria across the entire system lifetime. The close monitoring of equipment compliance to operating specifications helps identify possible effects due to external factors before spending valuable time and risking any impact on sample data. The naica® IQ/OQ Kit, the tool for routine OQ for Crystal Digital PCR™ Routine OQ procedures of the naica® system can be performed using the naica® IQ/OQ Kit, a ready-to-use OQ solution to gather the required documented verification that the naica® system is fully functioning according to its specifications to ensure stable analysis. Experience a streamlined, routine OQ solution with the naica® IQ/OQ Kit for a wide range of key nucleic acid detection and quantification applications. Figure 1. The naica® IQ/OQ Kit, a ready-to-use kit for the OQ of Crystal Digital PCR™ systems.

REACTION PREPARATION IMAGE ACQUISITION ANALYSIS & REPORT NAICA® SYSTEM OQ WORKFLOW Figure 2. Simple OQ workflow of Crystal Digital PCR™ systems with the naica® IQ/OQ Kit, a full OQ solution from reaction preparation to reporting of OQ results. The naica® IQ/OQ Kit can be included in your OQ routine process in compliance to global standards and country-specific regulations. OQ with the naica® IQ/OQ Kit is ideal for the monitoring of the naica® system on a periodic basis in accordance with established Standard Operating Procedures (SOPs). ONCOLOGY PATIENT MONITORING QUALITY CONTROL ENVIRONMENTAL...