UserName
Production validation services provide technical assistance through specialized products and programs. These services help ensure production processes meet required standards and specifications before full-scale manufacturing begins. Production validation services typically include testing, quality assurance, and verification activities to validate that production methods, equipment, and outputs are functioning correctly and efficiently.
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.
Service Offering | IQ/OQ/PQ with completion of documents |
---|---|
Type de produit | IQ/OQ Documentation (PDF) |
Gamme de produits | BINDER Chambers |
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
Service Offering | Supporting documents for validation performed by customers |
---|---|
Durée | On request |
Comprend | IQ/OQ checklists include calibration guide and comprehensive unit documentation |
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
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
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
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.
Gamme de produits | BINDER Chambers |
---|---|
Durée | On request |
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.
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.
À utiliser avec (équipement) | aCOLyte Instruments |
---|---|
À utiliser avec (application) | Instrument Validation |
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.
Service for performing IQOQ procedure for Sapphire FL Biomolecular Imager
IQ/OQ documentation for Sapphire FL Biomolecular Imager and associated fluorescent optical modules. Includes Procedure, Checklist and Logbook, Azure Test Targets, and Certificates.
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.
À utiliser avec (équipement) | ProtoCOL 3 Instruments |
---|
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.
À utiliser avec (équipement) | ChromaZona Instruments |
---|---|
À utiliser avec (application) | Instrument Validation |
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.
À utiliser avec (application) | Instrument Validation |
---|
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.
À utiliser avec (équipement) | ProcScan Instruments |
---|---|
À utiliser avec (application) | Instrument Validation |