Примери за използване на Shall be described 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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(2) In the tax-insurance account shall be described.
The methods shall be described in the own-risk assessment.
In that case, the mode of action of this toxin shall be described.
Each document from the register shall be described with one record(line) in the file.
The following pharmacokinetic characteristics shall be described.
(4) The protocols under para 1 and 2 shall be described in the sales record for the respective tax period.
Where possible, appropriate management strategies shall be described.
It shall be described as:‘Water consumption“X” litres per year, based on 280 standard cleaning cycles.
The pharmacodynamic action not related to efficacy shall be described.
Hazard of the NCS shall be described clearly in SDS, and SDS shall be passed to the downstream users;
The distribution of the medicinal product in the target animal shall be described;
Each document from the record shall be described with one record(line) in the file“PRODAGBI. ТХТ” with the following structure.
The origin and history of starting materials shall be described and documented.
All the needs shall be described, regardless whether they will be addressed through the CAP Strategic Plan or not;
The sources of the revenue included in the'all other segments' category shall be described.
The projects applying to be included in the Road Map shall be described in accordance with the form project description- Annex 2.
Where known, the expected effects and the duration of these effects following poisoning shall be described.
Each delivered vehicle shall be described with one record(line) in the file and shall be positioned on one magnetic or optical carrier.
The origin, including geographical region, and history of starting materials shall be described and documented.
These circumstances shall be described in a protocol on the type and the quantity of the goods abandoned to the State, and in the Fiscal Control register.
In the refund application, the nature of the goods and services acquired shall be described by the following codes.
All trials shall be described in sufficiently precise details so as to be reproducible in control trials, carried out at the request of the competent authorities.
The positive and negative effects, both technological and biological, shall be described for each experiment.
(e)"The assay technique(s)" shall be described in sufficiently precise detail to be reproducible in control tests carried out at the request of the competent authority;
Any special apparatus andequipment having been used shall be described in adequate detail.
(e) For cell-based products derived from genetically modified animals, the specific characteristics of the cells related to the genetic modification shall be described.
Constituents which are not given in any pharmacopoeia shall be described in the form of a monograph under the following headings.
Contraindications associated with particular regimes, particularly those relating to‧general medical problems‧ and conditions, shall be described.
The protocol shall be described in the purchases record of the issuer in file“POКUPKI. ТХТ” of the issuer, in the way a received debit invoice notice is being described. .
For allergen products, the specifications and control methods for the source materials shall be described in as much detail as possible.