Services de validation de production
Les services de validation de la production fournissent une assistance technique par le biais de produits et de programmes spécialisés. Ces services permettent de s'assurer que les processus de production respectent les normes et les spécifications requises avant le début de la fabrication à grande échelle. Les services de validation de la production comprennent généralement des activités de test, d'assurance qualité et de vérification pour valider que les méthodes de production, l'équipement et les résultats fonctionnent correctement et efficacement.
Services de validation de la production
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
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.
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 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
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.
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
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.
Azure Biosystems
Service for performing IQOQ procedure for Sapphire FL Biomolecular Imager
Synbiosis™ Synoptics
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™ Synoptics
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.
Synbiosis™ Synoptics
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.
Syngene™ Synoptics
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.
Azure Biosystems
IQ/OQ documentation for Sapphire FL Biomolecular Imager and associated fluorescent optical modules. Includes Procedure, Checklist and Logbook, Azure Test Targets, and Certificates.
Synbiosis™ Synoptics
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™ Synoptics
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.