Examples of using Documentation must in English and their translations into Slovak
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Colloquial
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Official
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Medicine
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Financial
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Ecclesiastic
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Official/political
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Computer
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Programming
Documentation must be accessible to the public.
Everything changes with time and all documentation must be kept up to date.
All documentation must be originals(no copies accepted).
In the case of PPE models referred to in Article 8(2), the documentation must comprise in particular.
The documentation must, so far as they are relevant to assessment, include.
These transfers must be documented and the documentation must be made available to the supervisory authority on request.
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.
Each documentation must be translated into the Albanian language and certified by a notary public!
Tables of prices or other tables and illustrations taken from the medicinal journals orother scientific works that are used in the documentation must be correctly reproduced and must state the exact source.
This documentation must enable the supervisory authority to verify compliance with this Article.
All pre-clinical and clinical documentation must be sufficiently detailed to enable an objective judgement to be made.
The documentation must be accompanied by photographic documentation of the manufacturing of the jewelry.
A firm must document allmajor changes in the risk rating process, and such documentation must support identification of changes made to the risk rating process subsequent to the last review by the appropriate regulator.
The documentation must be made available to the contractual parties and to members of health professions.
The submitted lamp or documentation must include a legible label with the date of production.
This documentation must be sufficient to enable the supervisory authority to verify compliance with this Article and with Article 30.
The clinical evaluation and its documentation must continually be updated by its post-market surveillance information.
This documentation must be sufficient to enable the supervisory authority to verify compliance with this Article.
The clinical evaluation and its documentation must be actively updated with data obtained from the post-market surveillance.
That documentation must be updated regularly to ensure that the selection criteria remain valid.
Technical documentation must demonstrate the conformity of the constituents with the requirements of this Regulation.
Contractual documentation must be shared within the parties, use and sharing is permitted to the extent necessary;
Such documentation must be available to the Competent Authority for a period appropriate for the use to which the products are placed on the market.
The documentation must be accurate, complete and confirmed and validated by the CPC or Member State authorities of the catching vessels or traps.
Transfer documentation must include a set of information, data and facts which explain and show/ prove the method how transfer price was created.
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.
All accounting documentation must clearly identify the true nature of business transactions, assets and liabilities in conformity with relevant regulatory, accounting and legal requirements.
The relevant technical documentation must be available for at least 10 years after the partly completed machinery manufacturing date or batch production the last unit produced, and on request presented to the competent authorities of the Member States.
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.