Search Thermo Fisher Scientific
- Contáctenos
- Orden Rápida
-
¿No tiene una cuenta? Crear una cuenta
Search Thermo Fisher Scientific
There’s no time for downtime in your lab. More than 2,000 trained professionals make up one of the industry’s largest global service and support networks, ready to provide you assistance when needed. Built on more than 35 years of service expertise, our exceptional services and support solutions help keep labs up and running.
All CTS Xenon Electroporation Systems come with a standard one-year warranty. During the one-year system warranty period, all costs for travel or shipping, labor, and parts for repairs are covered.
Many customers choose to purchase an AB Assurance on-site service plan, which extends the standard one-year warranty for an additional year. A service plan can:
AB Assurance is our most popular instrument service plan because it takes the guesswork out of ensuring instrument uptime, from issue prevention to quick resolution. With the AB Assurance plan, if something goes wrong that can’t be diagnosed and repaired remotely, we come to your site to correct it. The plan includes guaranteed response times in most regions, scheduled planned maintenance, and automatic software updates. Parts, labor, travel, and shipping are included.
Service aspect |
AB Assurance plan |
---|---|
Field repair response time |
2 business days* |
Planned maintenance service |
✓ |
Access to remote technical support (Mon-Fri, standard business hours) |
✓ |
Parts, labor, and travel |
✓ |
Qualification services |
Available as add-on |
Field application scientist (FAS) consultation |
Available as add-on |
*Response times vary by region.
During the second year of the AB Assurance plan, our field service engineer (FSE) will visit your site to perform a scheduled planned maintenance (PM). Maintenance visits are intended to help you prevent downtime, reduce strain on your laboratory staff, and help ensure the life of your instrument.
During a PM service visit, the FSE will inspect the system, update the software if required, and clean, lubricate, and calibrate relevant mechanical parts. The FSE will also complete functional tests and performance verification and document maintenance tasks, results, and findings.
Service plans may be purchased** along with your CTS Xenon Electroporation System as detailed in the instrument/service plan bundles below. For a system you’ve already purchased, extended warranties covering an extra year are also available. Contact your local sales representative regarding an extra year of service.
**Extended warranty packages are not available in all regions. Please contact your local sales representative or contact us.
You can add qualification services to complement your service plan. Instrument hardware qualifications for the CTS Xenon Electroporation System document and verify that the instrument is installed and operating properly.
Instrument qualification (IQ) provides documented evidence and verification that the instrument has been delivered and installed according to the manufacturer’s specifications.
Operational qualification (OQ) provides documented verification that the instrument subsystems are operating as designed and verifies that the functionality of an instrument meets the manufacturer’s operational specifications.
IQ and OQ are recommended at installation, after moving the instrument, after software or hardware upgrades, and after planned maintenance or critical repairs. Our qualification specialists will partner with you to help deliver timely, cost-effective, and trusted qualification services that include reliable, audit-style documentation that can help ensure your instruments meet regulatory requirements.
AB qualification service provides a second on-site Operational Qualification service visit with a field service engineer (FSE) within two years of installation. This OQ is required after major preventative maintenance, an instrument move, or other significant change. The FSE runs prescribed tests using a protocol designed to challenge the operating parameters of the instrument to help ensure it functions within design specifications. The FSE evaluates and documents the test results and determines pass/fail. Upon receiving a pass result, the FSE verifies the instrument is operating within the manufacturer’s design specifications. AB Qualification documentation may be included in a device history file to be referenced during audits and inspections as part of risk mitigation strategies.
For Research Use or Manufacturing of Cell, Gene, or Tissue-Based Products.