Examples of using Human use in English and their translations into Danish
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Medicine
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Colloquial
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Official
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Financial
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Ecclesiastic
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Official/political
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Computer
Easotic(Hydrocortisone Aceponate/Miconazole Nitrate/Gentamicin Sulfate) is only meant for use in dogs and is not for human use.
Easotisk(Hydrocortison Aceponate/ Miconazol Nitrat/ Gentamicinsulfat) er kun beregnet til An updated Risk Management Plan should be provided as per the CHMP guideline on Risk Management Systems for medicinal products for human use.
En opdateret Risk Management Plan bør være vedlagt i henhold til CHMP Guideline om Risk Management Systemer for lægemidler til human anvendelse.Council Recommendation 83/571/EEC contains notes for guidance on the conduct of certain tests and trials for proprietary medicinal products for human use.
Rådets henstilling 83/571/EØF indeholder retningslinjer for gennemførelse af visse undersøgelser vedrørende medicinske specialiteter til menneskebrug.This should be in line with the CHMP Guideline on Risk Management Systems for Medicinal Products for Human use and should be submitted within 30 days after the Commission Decision.
Dette skal følge CPMP Guideline for Risk Management Systems for Medicinal Products for Human Use and skal indsendes inden 30 dage efter Commission Decision.Easotic(Hydrocortisone Aceponate/Miconazole Nitrate/Gentamicin Sulfate) is only meant for use in dogs and is not for human use.
Easotic(Hydrocortisonaceponat/ Miconazolnitrat/ Gentamicin sulfat) er kun beregnet til which will strengthen her ground-breaking research into user interfaces for the complex human use of computers.
som skal styrke hendes banebrydende forskning i brugergrænseflader for kompleks menneskelig brug af computere.An updated Risk Management Plan should be provided as per the CHMP Guideline on Risk Management Systems. for medicinal products for Human Use.
En opdateret Risk Management Plan skal udarbejdes i henhold til CHMP' s retningslinjer for Risk Management Plan for lægemidler til human anvendelse.commercialise this peptide for human use in a cosmetic product.
markedsføre dette peptid til human brug i et kosmetisk produkt.treatments intended for human use.
behandlinger godkendt til brug på mennesker.The Marketing Authorisation Holder will provide Periodic Safety Update Report every two years until otherwise decided by the Committee for Medicinal Products for Human Use CHMP.
Indehaveren af markedsføringstilladelsen vil indsende Periodic Safety Update Report hvert andet år indtil andet besluttes af Committee for Medicinal Products for Human Use CHMP.security of trenbolone for human use are being theorized from animal studies.
der bliver teoretiseret resultaterne samt sikkerhed trenbolon til human anvendelse fra dyreforsøg.also has been approved by theFDA for human use.
er blevet godkendt af theFDA for menneskelige forbrug.is unsafe for human use.
er farligt til brug på mennesker.An updated Risk Management Plan should be provided as per the CHMP guideline on Risk Management Systems for medicinal products for human use.
En opdateret Risk Management Plan skal fremsendes som beskrevet i CHMP Guideline on Risk Management Systems for medicinal products for human use.the product is tested to be safe for human use.
er produktet testet til at være sikker til human brug.the implications of the nonclinical findings for the safe human use of the pharmaceutical should be discussed pananglitan,
konsekvenserne af de ikke-kliniske resultater til sikker human anvendelse af det farmaceutiske bør diskuteres dvs.,also has actually been accepted by theFDA for human use.
af Winthrop Laboratories(Sterling Drug) i 1962, samt har været godkendt af theFDA for menneskelige forbrug.An updated Risk management should be provided as per the CHMP guideline on Risk Management System for medicinal products for human use.
Et opdateret Risk Management system skal frembringes i forhold til CHMP guideline on” Risk Management Systems for medicinal products for human use”.As per the CHMP Guideline on Risk Management Systems for medicinal products for human use, the updated RMP should be submitted at the same time as the next Periodic Safety Update Report PSUR.
Ifølge CHMP retningslinjer for risikostyringssystemer for medicinske produkter til humant brug, skal den opdaterede risikostyringsplan indsendes på samme tidspunkt som den næste Periodiske Sikkerhedsopdaterede Rapport.An updated Risk Management Plan should be provided as per the CHMP guideline on Risk Management Systems for medicinal products for human use.
En opdateret Risk Management Plan skal tilvejebringes som ifølge CHMP Guideline on Risk Management Systems for lægemiddelprodukter til human anvendelse.
