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    CONCLUSION NO 36: EMISSION PREMIUM FOR EXCESS CO2 EMISSIONS

    Secinājums Nr. 36. Maksa par pārsniegtajām CO2 emisijām
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    Technical documentation and requirements

    IAF MD 9 Application of ISO/IEC 17021 in Medical Devices QMS (ISO 13485)

    IAF MD 9 IAF obligātais dokuments ISO/IEC 17021-1 piemērošana medicīnisko ierīču kvalitātes pārvaldī
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    Technical documentation and requirements

    Coaching Youth Initiatives. Guide for Supporting Youth Participation

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    Guidelines

    Functional Guidelines (AVCI) for Automated Vehicle and Container Identification system (AVCI) to be deployed at the new EU external landborders

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    Guidelines

    FMVSS 205 Glazing materials

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    Technical documentation and requirements

    CONCLUSION NO 37: TREATMENT OF PAYMENT FOR ACTIVATING AN ADDITIONAL SOFTWARE FUNCTION OF GOODS AFTER RELEASE FOR FREE CIRCULATION

    Secinājums Nr. 37. Rīcība ar maksājumu par papildu programmatūras funkcijas aktivizēšanu pēc preču l
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    Technical documentation and requirements

    Laboratory Documentation Packages

    WADA tehniskais dokuments, Laboratorijas dokumentācijas pakete
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    Technical documentation and requirements

    Communication from the Commission — Notice — Guidelines on the application of Article 81(3) of the Treaty

    Paziņojums Pamatnostādnes par Līguma 81. panta 3. punkta piemērošanu (2004/C 101/08)
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    Guidelines

    General Guidance for Consignments of Live Animals

    VISPĀRĪGI NORĀDĪJUMI PAR DZĪVU DZĪVNIEKU UN DZĪVNIEKU IZCELSMES PRODUKTU TRANZĪTA SŪTĪJUMIEM VAI PĀR
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    Guidelines

    FMVSS 209 Seat belts assemblies

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    Technical documentation and requirements

    Harmonization of Analysis and Reporting of Erythropoiesis Stimulating Agents (ESAs) by Electrophoretic Techniques

    WADA tehniskais dokuments, Eritropoēzi stimulējošu līdzekļu (ESA) analīžu ar elektroforētiskajām met
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    Technical documentation and requirements

    "Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use Annex 1"

    "4. sējums ES vadlīnijas labai ražošanas praksei Cilvēkiem paredzētās un veterinārās zāles I daļa 1.
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    Guidelines

    CPA Introductory Guidelines: the methodological guidelines for applying the Statistical classification of products by activity (CPA)

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    Guidelines

    Guidance Note Interpretation of Regulation 17742002EC Questions arising from FVO inspections to Member States (2004-2005)

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    Guidelines

    Model Requirements for the Management of Electronic Records: Update and Extension, 2008

    ELEKTRONISKO IERAKSTU PĀRVALDĪBAS PARAUGPRASĪBAS
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    Technical documentation and requirements

    Human Growth Hormone (hGH) Isoform Differential Immunoassays for Doping Control Analyses

    WADA tehniskais dokuments, Cilvēka augšanas hormona (hGH) izoformu diferenciālie imūntesti dopinga k
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    Technical documentation and requirements

    "Volume 4 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use Annex 20"

    "4. sējumsES vadlīnijas labai ražošanas praksei Cilvēkiem paredzētās un veterinārās zāles 20. pielik
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    Guidelines

    Development of test guidelines (TGP/7)

    Dokuments TGP/7
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    Guidelines

    Guidance Note on Fraud Indicators for ERDF, ESF and CF

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    Guidelines

    An economic assessment of GHG mitigation policy options for EU agriculture

    SEG emisiju mazināšanas politikas iespēju ekonomiskais novērtējums ES lauksaimniecības nozarē
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    Technical documentation and requirements