medicines oor Slowaaks

medicines

naamwoord
en
Plural form of medicine.

Vertalings in die woordeboek Engels - Slowaaks

lieky

Does the medicine act quickly?
Účinkuje ten liek rýchlo?
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chemoterapeutiká

AGROVOC Thesaurus

medikamenty

Dean, I need some of that non-drowsy allergy medicine stuff.
Dean, potrebujem niečo s tých neospalých alergických medikamentov.
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terapeutické látky

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veterinárne liečivá

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements
Všetok nepoužitý veterinárny liečivý prípravok alebo odpad, ktorý pochádza z tohto prípravku, musí byť zlikvidovaný podľa miestnych právnych predpisov
AGROVOC Thesaurus

Geskatte vertalings

Vertoon algoritmies gegenereerde vertalings

Soortgelyke frases

physical medicine and rehabilitation
Fyziatria, balneológia a liečebná rehabilitácia
medicinal finger
prstenník
medicinable finger
prstenník
forensic medicine
súdne lekárstvo · súdne lekárstvokulptur
hyperbaric medicine
Hyperbarická kyslíková terapia
traditional medicine
Ľudové liečiteľstvo
herbal medicine
bylinkárstvo · fytoterapia
medicinal plants
farmaceutické rastliny · liečivky · liečivé byliny · liečivé rastliny
preventative medicine
Profylaxia

voorbeelde

Advanced filtering
Voorbeelde moet herlaai word.
(76) Radiodiagnostic means pertaining to in-vivo diagnostic nuclear medicine, medical diagnostic radiology using ionising radiation, and dental radiology;
V prílohe možno uviesť akékoľvek hodnotenia potenciálu energie z obnoviteľných zdrojov vašej krajinyEurLex-2 EurLex-2
the unique identifier was decommissioned earlier than the time of supplying the medicinal product to the public, pursuant to Articles 23, 26, 28 or 41;
% 3⁄4udí v tomto štádiu už neberie inzulínEurLex-2 EurLex-2
NAME, PHARMACEUTICAL FORM, STRENGTH OF THE MEDICINAL PRODUCT, ANIMAL SPECIES, ROUTES OF ADMINISTRATION AND MARKETING AUTHORISATION HOLDER
AKO UCHOVÁVAŤ LISONORMEurLex-2 EurLex-2
Article 17 of Regulation (EC) No 470/2009 requires that the maximum residue limit (‘MRL’) for pharmacologically active substances intended for use in the Union in veterinary medicinal products for food-producing animals or in biocidal products used in animal husbandry is established in a Regulation.
Je to len chytrák, tulákeurlex-diff-2018-06-20 eurlex-diff-2018-06-20
The Agency shall be responsible for coordinating the existing scientific resources put at its disposal by Member States for the evaluation, supervision and pharmacovigilance of medicinal products.
Pri plánovaní gravidity, ako aj počas gravidity sa odporúča intenzívna kontrola gravidných žien s diabetes mellitusEurlex2019 Eurlex2019
Wholesale distributors must ensure they supply medicinal products only to persons who are themselves in possession of a wholesale distribution authorisation or who are authorised or entitled to supply medicinal products to the public.
PRIJALA TOTO ROZHODNUTIEEurLex-2 EurLex-2
Objective #14: An intensified exchange of information on illegal distribution channels in relation to counterfeit medicinal products should be proposed by 2012.
A.# Zachovanie preukazu spôsobilosti technika údržby lietadielEurLex-2 EurLex-2
A link to the national and Community safety web portals would allow patients to access additional information about the safety of a medicinal product.
Každý účastník konania znáša vlastné trovy konanianot-set not-set
6 Summary of the characteristics of the veterinary medicinal product(s) prepared in accordance with Article 5a of Directive 81/851/EEC.
Ukazovatele sociálneho vylúčenia a chudobyEurLex-2 EurLex-2
In their opinion, the fact that the use of medicine is generally subject to external examination by health professionals (including doctors, nurses or pharmacists) and that the producer does not have any control over the way in which medicines are prescribed or administered should be taken into account when analysing the defect of the product and the producer’s liability.
prášok na injekčný roztokEurLex-2 EurLex-2
The particulars mentioned in paragraph 1(f) to (l) shall appear on the outer package and on the container of the medicinal products in the language or languages of the country in which they are placed on the market.
To čo ste mi spoločne spraviliEurLex-2 EurLex-2
whereas most of today’s high-tech industries use this technology, whereas opportunities to use 3D printing have highly increased in many areas, and whereas expectations are high in many areas, for example the medical (ranging from regenerative medicine to the manufacture of prosthetics), aeronautics, aerospace, automotive, household electrical appliance, building, archaeological research, architecture, mechanical engineering, leisure and design sectors;
názvy a presný opis činností všetkých prepojených spoločností, ktoré sú zapojené do výroby a/alebo predaja (na vývoz a/alebo na domácom trhu) výrobku, ktorý je predmetom prešetrovaniaEuroParl2021 EuroParl2021
The proposals include an assessment at EU level of the added therapeutic value of health technologies and the harmonisation of the criteria used in clinical trials of medicinal products in order to improve the level of clinical evidence, encourage high-quality innovation and make it possible to identify technologies which offer genuine added value.
so zreteľom na článok # ods. #, článok # ods. # a článok # Zmluvy o ES, v súlade s ktorými Komisia predložila návrh Parlamentu (Cnot-set not-set
However, it should be stressed that innovative medicines produce considerable economic benefits including:
Sociálna politikaEurLex-2 EurLex-2
Retailing or selling via global computer networks of surgical and medical dental and veterinary nuclear medicine diagnostic imaging apparatus in the nature of gamma cameras
Spomedzi týchto # pacientov # už absolvovalo skenovanie použitím štandardnej scintigrafickej metódy (keď pacient dostáva osobitne pripravenú injekciu vlastných bielych krviniek rádioaktívne značených a vhodným rádioaktívnym značkovacím izotopomtmClass tmClass
Articles 66 and 67 shall not apply to radiopharmaceuticals used as diagnostic investigational medicinal products or as diagnostic auxiliary medicinal products.
zaťaženie musí byť chránené pred prachomEurLex-2 EurLex-2
... at the moment the period that elapses between the filing of an application for a patent for a new medicinal product and authorisation to place the medicinal product on the market makes the period of effective protection under the patent insufficient to cover the investment put into the research;
Myslím, že ide ku mneEurLex-2 EurLex-2
A contrary interpretation would constitute interference in the organisation by Member States of their domestic social security policies and affect the Member States’ policies for pricing medicinal products to an extent going beyond what is necessary to ensure transparency for the purposes of Directive 89/105.
Aké riziká sa spájajú s užívaním lieku Zyprexa?EurLex-2 EurLex-2
An application for a modification of the existing entry for aluminium salicylate, basic, has been submitted to the European Medicines Agency (hereinafter ‘EMA’).
Je ochotný odpustiť z trestu, ak pristúpite k dohodeEurLex-2 EurLex-2
(a) a marketing authorisation for the veterinary medicinal product to be administered to the animals has been granted by the competent authorities of the Member State in which the veterinarian is established or by the Commission;
Fyzické alebo právnicke osoby, ktoré spĺňajú podmienky stanovené v pravidlách o účasti, a na ktoré sa v pravidlách o účasti alebo v článku # ods. # nariadenia Rady (ES, Euratom) č. #/# z #. júna # finančného naria denia uplatniteľného na všeobecný rozpočet Európskych spoločenstiev (ďalej len navrhovatelia) nevzťahuje žiaden prípad o vylúčení, sú, v prípade, že sú podmienky pravidiel o účasti a príslušnej výzvy splnené, prizvané predložiť Komisii návrhy na nepriame akcie RTDnot-set not-set
coordinating the monitoring of medicinal products for human use which have been authorised within the Union and providing advice on the measures necessary to ensure the safe and effective use of these medicinal products for human use, in particular by coordinating the evaluation and implementation of pharmacovigilance obligations and systems and the monitoring of such implementation;
Aj keby boli clá zavedené v plnej výške, v najhoršom prípade by to viedlo k zvýšeniu o nie viac ako # % nákladov poľnohospodárovEurLex-2 EurLex-2
By ..., a Paediatric Committee shall be established within the European Medicines Agency set up under Regulation (EC) No #/#, hereinafter 'the Agency'
Predávkovanieoj4 oj4
Transport, storage and distribution of medicines and medicinal preparations
Počas OP bol trh Spoločenstva týkajúci sa príslušného výrobku a podobného výrobku približne na rovnakej úrovni ako v roku #, t. j. vo výške približne # tontmClass tmClass
Commission Regulation (EC) No #/# of # November # amending Annex I to Council Regulation (EEC) No #/# laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards Monensin, Lasalocid and Tylvalosin
Píše do svojej knihy a slová sa objavia v tejtooj4 oj4
We are voting in favour, however, since measures are being introduced to make sure that imported pharmaceutical products are safer, including traceability, a ban on repackaging, compliance with EU safety standards, the partial regulation of Internet sales, and the possibility of extending similar measures to over-the-counter medicinal products as well.
Členské štáty by v spolupráci s Komisiou mali vytvoriť komplexnú podpornú sieť s cieľom pomôcť spoločnostiam a najmä MSP splniť požiadavky tohto nariadeniaEuroparl8 Europarl8
205 sinne gevind in 4 ms. Hulle kom uit baie bronne en word nie nagegaan nie.