9238815Rect. carrier for 12 tubes 10 ml w/ capCNY
9019472TAPE SPACER CLEAR GSCNY
9019464UV tube, CxxCNY
9243650Comprehen Valid., EZ1/QIAcube/QIAsymph"""The Comprehensive Validation Support plan specific to a laboratory＇s needs will incorporate all of the requirements for the internal validation guidelines from the FBI＇s Quality Assurance Standards (QAS).
The Comprehensive Validation Support service includes all travel ａnd labor charges for up to 20 days by the QIAGEN Validation Team. Typically, one week will be required to extract, quantify, ａnd amplify the validation study samples ａnd may require multiple individuals. Usually, two weeks is required to analyze the data ａnd one week to write the final report. The expected time period to complete the Comprehensive Validation is six weeks. The actual time may vary depending on resource availability, including laboratory time dedicated to validation activities.
Lab Work – The QIAGEN specialist(s) will travel to the laboratory to conduct the on-site validation lab work. The QIAGEN specialist team will perform ａnd complete all extractions, quantifications, amplfications, ａnd capillary electrophoresis. The laboratory is responsible for providing systems/protocols that may be needed (generally laboratory SOPs, ex. interpretation guidelines). Additionally, the laboratory staff may be required to provide additional data needed for interpretation (ex. quantification/amplification/CE results) during the data review phase of the validation.
Once the final scope of the validation is determined, QIAGEN will provide a quote for all consumables required for the validation. Non-QIAGEN chemistry ａnd accessories are not included ａnd should be purchased to cover the validation experimental design including qPCR, STR, NIST standards, required samples types (blood, semen, buccal samples) ａnd required substrates (swabs, materials, etc). The Customer is expected to have all materials on-hand 1 week prior to the validation start date.
Data Analysis – The Comprehensive Validation Support plan encompasses data collection (quants, amps, CE) during the on-site visit. The laboratory may be responsible for sharing (typically electronically via e-mail) any validation data requested after the on-site visit. A QIAGEN specialist will complete all of the data analysis produced from the validation study design. This includes qPCR (quant) ａnd STR (amp) analysis ａnd linkage to starting samples.
Validation data CD/flashdrive – QIAGEN will review the validation data ａnd draft a validation summary document, ensuring compliance with the FBI＇s QAS requirements/standards. QIAGEN will send validation data in an electronic format (email/CD/flashdrive) to the laboratory. The laboratory is responsible for final compilation, any format change preferences, review ａnd signoff of the validation report. The documentation provided by QIAGEN will aide in demonstrating compliance with all accreditation guidelines during laboratory audits. Should a hard copy of the validation study be preferred, the laboratory is required to specify prior to the onset of the validation.
Post-validation QIAGEN-to-Laboratory Transfer – Following completion of the validation ａnd generation of the draft validation summary document, a designated member of the QIAGEN validation team will review the validation with the Lab Manager ａnd the Technical Leader. Following sign off on the validation report, training of the laboratory DNA staff will occur. Refer to the Post-validation Competency Training for additional information. """CNY
9237333Install, BR plus 3 integr. w. schedulingInstallation ａnd training, BioRobot System including three approved integration devices with schedulingCNY
9237328Upgrade, BR & 2 ext. devices w. sched.Upgrade BioRobot with two approved integration devices using scheduling softwareCNY
9237173Shield, V-housingCNY
9233208Tubing, liquid system 2.5/1.5CNY
9237155V-Housing with Sample NeedleCNY
9237150Heater TopCNY
9016151#App. Package, M48, PathologyCNY
9019179Opto - plate lock closed, PyroQ96MDCNY
9011883Upgrade, high speed pipetting systemCNY
9011882Back unit, BR9600CNY
9011823Z-Modul; Tip-Adapter 300µl; BR8000CNY
92369163 Year Warranty, LiquiChipLiquiChip 3-year Warranty with 1 Preventive Maintenance per year. Included in system price. This warranty must be included as a line item on the system quote. It covers the system for three years total including all per incident travel ａnd labor charges, all repair parts, one preventive maintenance visits per year (three in total), ａnd 48- hour priority response.CNY
9019143Power supply, PyroQ96CNY
9019129Cable - Reagent, PyroQ96IDCNY
9019126PCB 2 - Connection, PyroQ96IDCNY
9019114IPC mainboard, PyroQ96IDCNY
9019025Worktable, side wall, left, EZ1xlCNY
9019012Motor Y, EZ1xlCNY
9018942Adapter, 2xRing of 12 COBAS AmplicoreCNY
9022737Rotor-Gene AssayManager SOWCNY
9016061Tubing Set, Syringe inlet, BR8000 ICNY
9015823CD, Field Syringe Calibration, BR8000CNY
9015690Rings (10), pinching, 4.5/3.2 mmCNY
9015599CD, Manual, Service, BIOROBOT 8000 IICNY
9015587EZ1 DNA Buffy Coat CardPre-programmed card for BioRobot EZ1 DNA Buffy Coat ProtocolCNY
9019166Lead screw - X, PyroQ96MDCNY
