Примери за използване на Documentation must на Английски и техните преводи на Български
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Computer
What documentation must accompany the application?
Everything changes with time and all documentation must be kept up to date.
All documentation must be sent before October 10, 2019.
For devices intended for clinical investigations, the documentation must contain.
All documentation must be kept in Germany, in German.
Хората също превеждат
For devices intended for clinical investigations, the documentation must contain.
The documentation must contain the name, address and ownership.
Where appropriate, the design documentation must contain the following elements:-.
All documentation must necessarily be translated. in Thai and notarized.
In the case of PPE models referred to in Article 8(2), the documentation must comprise in particular.
Such documentation must be kept up to date and be available.
In the case of PPE models referred to in Article 8(2), the documentation must comprise in particular.
By Ba documentation must be maintained for at least 4 years.
Any damages to the packaging and/or the Product ordiscrepancies in the number of items or documentation must be immediately indicated in writing on the Courier's delivery note.
This documentation must be available to the border veterinary authorities. Currency.
All references and any supporting documentation must be sent as part of your full application.
The documentation must also contain a customer declaration as referred to in Article 4.
Before the demolition of the partition, it is necessary to prepare a draft redevelopment andobtain a technical conclusion, after which the documentation must necessarily pass the approval procedure in the housing inspection.
The documentation must show which requirements of this Directive are applied and fulfilled.
All pre-clinical and clinical documentation must be sufficiently detailed to enable an objective judgement to be made.
The documentation must allow an understanding of the design, the manufacture and the performances of the product.
This supporting documentation must describe how the principles in RFC1591, ICP-1, and the GAC principles are supported.
The documentation must make it possible to understand the design, the manufacture and the performances of the product.
The documentation must make it possible to assess the electrical equipment's conformity to the relevant requirements.
This documentation must be sufficient to enable the supervisory authority to verify compliance with this Article and with Article 30.
Such documentation must be available to the competent authorities for a period appropriate for the use to which the products are placed on the market.
Ideally, the design documentation must be requested from the experts, but you can use ready-made projects, placed on the Internet or borrowed from friends.
The documentation must allow an understanding of the design, the manufacture and the performances of the product and must contain the following items in particular.
The relevant technical documentation must be available for at least 10 years following the date of manufacture of the partly completed machinery or, in the case of series manufacture, of the last unit produced, and on request presented to the competent authorities of the Member States on request.
The relevant technical documentation must be available for at least 10 years following the date of manufacture of the partly completed machinery or, in the case of series manufacture, of the last unit produced, and on request presented to the competent authorities of the Member States.