Production Validation Services
Production Validation Services
BINDER™ Qualification Documents IQ/OQ
Qualification documents - Digital in PDF format, IQ/OQ documents – supporting documents for validation performed by customers, consisting of: IQ/OQ checklists including calibration guide and comprehensive unit documentation.
BINDER™ Qualification Documents IQ/OQ /PQ
Qualification documents - IQ/OQ/PQ documents – supporting documents for validation performed by customers, according to customer requirements, PQ section added to qualification folder IQ/OQ; parameters: temperature, CO2, O2 – or pressure, depending on unit.
BINDER™ Qualification Documents IQ/OQ
Qualification documents - IQ/OQ documents – supporting documents for validation performed by customers, consisting of: IQ/OQ checklists incl. calibration guide and comprehensive unit documentation; parameters: temperature, humidity, and light values
Unity Lab Services™ Thermo Scientific™ Centrifugation Validation Service
Stay compliant with our Industry-Exclusive, No-Charge Requalification Guarantee included with each Thermo Scientific Centrifugation Validation Service for Benchtop, Micro, Bioprocessing, Clinical, and Standard floor model centrifuges: Thermo Scientific, Sorvall
Unity Lab Services™ Thermo Scientific™ Liquid Nitrogen Storage Equipment Validation Service for Thermo Scientific™ CryoMed™ Controlled-Rate Freezers
Stay compliant with our Industry-Exclusive, No-Charge Requalification Guarantee included with each Thermo Scientific Liquid Nitrogen Storage Equipment Validation Service for Thermo Scientific CryoMed™ Controlled-Rate Freezers
Unity Lab Services™ Thermo Scientific Liquid Nitrogen Storage Equipment Validation Service with Temperature Mapping for CryoPlus™ Storage Systems
Stay compliant with our Industry-Exclusive, No-Charge Requalification Guarantee included with each Thermo Scientific Liquid Nitrogen Storage Equipment Validation Service with Temperature Mapping for Thermo Scientific CryoPlus™ Storage Systems
Eppendorf™ Centrifuge Services - IQ/OQ - GxP
GxP compliant IQ/OQ documentation support the complex GxP standards and regulations reducing your administrative workload, and provide you with qualified assurance that your instrument is installed and is operating in accordance with manufacturers' specifications.
Synbiosis™ Protos 3 Instrument Validation Procedures
Protos 3 Instrument Validation Procedures take the user through each step in the verification of a Synbiosis™ system regulatory compliances and standard operational procedures (SOP). These simple procedures allow the user to verify that a system meets defined installation, operational, and performance quality specifications.
Syngene™ G:BOX F3 Instrument Validation Procedures
G:BOX F3 Instrument Validation Procedures take the user through each step in the verification of a Synbiosis™ system regulatory compliances and standard operational procedures (SOP). These simple procedures allow the user to verify that a system meets defined installation, operational, and performance quality specifications.
Synbiosis™ ProtoCOL 3 Instrument Validation Procedures
ProtoCOL 3 Instrument Validation Procedures take the user through each step in the verification of a Synbiosis™ system regulatory compliances and standard operational procedures (SOP). These simple procedures allow the user to verify that a system meets defined installation, operational, and performance quality specifications.
Synbiosis™ aCOLyte Instrument Validation Procedures
aCOLyte Instrument Validation Procedures take the user through each step in the verification of a Synbiosis™ system regulatory compliances and standard operational procedures (SOP). These simple procedures allow the user to verify that a system meets defined installation, operational, and performance quality specifications.
Synbiosis™ ProcScan 3 Instrument Validation Procedures
ProcScan 3 Instrument Validation Procedures take the user through each step in the verification of a Synbiosis™ system regulatory compliances and standard operational procedures (SOP). These simple procedures allow the user to verify that a system meets defined installation, operational, and performance quality specifications.
Synbiosis™ ChromaZona Instrument Validation Procedures
ChromaZona Instrument Validation Procedures take the user through each step in the verification of a Synbiosis™ system regulatory compliances and standard operational procedures (SOP). These simple procedures allow the user to verify that a system meets defined installation, operational, and performance quality specifications.
Azure Biosystems Sapphire FL IQ/OQ Documentation
IQ/OQ documentation for Sapphire FL Biomolecular Imager and associated fluorescent optical modules. Includes Procedure, Checklist and Logbook, Azure Test Targets, and Certificates.
Azure Biosystems Sapphire FL IQOQ Service
Service for performing IQOQ procedure for Sapphire FL Biomolecular Imager