ebro Winlog.validation Software
#Grup produk P106648809
Spesifikasi
Hardware Requirements | Processor: Pentium 1 GHz, Main memory: 1 GB, Free hard disk space: 1 GB, USB |
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Software Requirements | Windows Vista (32 bit or 64 bit), Windows 7,8,10 (32 bit or 64 bit) |
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Informasi Produk
Description
Save time and effort for the regularly required process validation with the help of the powerful reporting and evaluation software Winlog.validation.
The automatic recognition of the individual process steps makes your work easier and meets the high demands of validation and qualification in pharmacy and medicine.
The TÜV-certified evaluation software Winlog.validation enables you to carry out automatic and manual evaluations of the processes. You can adapt it to your needs at any time with individual process parameters and test criteria.
• TÜV certified
• User-friendly - DIN EN ISO 9241-110:2008 conform
• Central user administration in local area network possible
• Automatic report generation
• Automatic user-defined calculations
• Automatic identification of process cycles
• Creation of user-defined masters for specific devices and
thermal processes
• Three-dimensional demonstration of sensor placement or placement of
the sensors directly on an application image possible
• FDA 21 CFR Part 11
• DIN ISO/IEC 25051:2014
• Incl. IQ- / OQ-Documentation for software Qualification
• Automatic evaluation of validation processes
The automatic recognition of the individual process steps makes your work easier and meets the high demands of validation and qualification in pharmacy and medicine.
The TÜV-certified evaluation software Winlog.validation enables you to carry out automatic and manual evaluations of the processes. You can adapt it to your needs at any time with individual process parameters and test criteria.
• TÜV certified
• User-friendly - DIN EN ISO 9241-110:2008 conform
• Central user administration in local area network possible
• Automatic report generation
• Automatic user-defined calculations
• Automatic identification of process cycles
• Creation of user-defined masters for specific devices and
thermal processes
• Three-dimensional demonstration of sensor placement or placement of
the sensors directly on an application image possible
• FDA 21 CFR Part 11
• DIN ISO/IEC 25051:2014
• Incl. IQ- / OQ-Documentation for software Qualification
• Automatic evaluation of validation processes
Ulasan Produk
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