Validation requirements for EPE models
Merchant and Service Provider Levels and Validation Requirements
Validation requirements for forming, sealing and assembly processes
It is not the intention to be prescriptive in specific validation requirements.
Comply with the Payment Card Industry Data Security Standard (PCI DSS) and the applicable validation requirements.
Refers to ISO 14064-3 for validation / verification requirements.
If the location data matches one of the predetermined locations and the specified approval requirements are met, then the purchase is approved.
UNB's Department of Chemical Engineering facilities are well-suited to Terrestrial Energy's validation and verification requirements.
UNB's Department of Chemical Engineering facilities are well-suited to Terrestrial Energy's validation and verification requirements.
Coverage begins on the date of arrival in Alberta, once all registration validation requirements are met.
NOTE 1 Requirements for validation and control of dry heat sterilization processes are provided by ISO 20857.
NOTE 1 Requirements for validation and control of moist heat sterilization processes are provided by the ISO 17665 series.
NOTE - Requirements for the validation and routine control of sterilization by moist heat are given in EN ISO 17665 1.
NOTE Requirements for the validation and routine control of sterilization by moist heat are given in EN ISO 17665 1.
Packaging for Terminally Sterilized Medical Devices - Part 2: Validation and Requirements for Forming, Sealing and Assembly Processes.
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
Packaging for Terminally Sterilized Medical Devices - Part 2: Validation and Requirements for Forming, Sealing and Assembly Processes.
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
Packaging for Terminally Sterilized Medical Devices - Part 2: Validation and Requirements for Forming, Sealing and Assembly Processes.
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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