Overview
This chapter contains BioTek Instrument's recommended qualification procedures for all
Synergy H1 models.
Every Synergy H1 is fully tested at BioTek prior to shipment and should operate properly
upon initial setup. If you suspect that a problem occurred during shipment, if you have
received the equipment after returning it to the factory for service, and/or if regulatory
requirements dictate that you qualify the equipment on a routine basis, perform the
procedures outlined in this chapter.
See the
Recommended Qualification Schedule
on page
to determine which qualification
tests shall be conducted for your Synergy H1 model and to meet your site's regulatory
requirements.
A Product Qualification Package (BTI #8040528) for the Synergy H1 is available for
purchase. The package contains test procedures, Gen5 protocols, checklists, and
logbooks for performing Installation Qualification, Operational Qualification,
Performance Qualification, and Preventive Maintenance. Contact your BioTek dealer for
more information.
If the gas controller module is used with the Synergy H1, refer to the
Gas Controller
User Guide
(BTI #1211000) or
Gas Controller Product Qualification Package
(BTI #1210512) for qualification procedures.
108 | Chapter 8: Instrument Qualification Procedures
BioTek Instruments, Inc.
Summary of Contents for Synergy H1
Page 1: ...Hybrid Multi Mode Microplate Reader Synergy H1 TM Operator s Manual ...
Page 2: ......
Page 26: ...BioTek Instruments Inc xxiv Preface ...
Page 54: ...BioTek Instruments Inc 28 Chapter 2 Installation ...
Page 68: ...BioTek Instruments Inc 42 Chapter 3 Getting Started ...
Page 132: ...BioTek Instruments Inc 106 Chapter 7 Instrument Qualification Process ...