Normy

Obsah

ČSN ETSI EN 319 411-2 V2.1.1 The present document specifies policy and security requirements for the issuance, maintenance and life-cycle management of EU qualified certificates as defined in Regulation (EU) N° 910/2014 [i.1]. These policy and security requirements support reference certificate policies for the issuance, maintenance and life-cycle management of EU qualified certificates issued to natural persons (including natural persons associated with a legal person or a website) and to legal persons (including legal persons associated with a website), respectively. The present document does not specify how the requirements identified can be assessed by an independent party, including requirements for information to be made available to such independent assessors, or requirements on such assessors. The present document however provides in annex B a check list of the policy requirements specific to TSP issuing EU qualified certificates (as expressed in the present document) as well as all the requirements incorporated by reference to ETSI EN 319 411-1 [2] and ETSI EN 319 401 [1], that can be used by the TSP to prepare an assessment of its practices against the present document and/or by the assessor when conducting the assessment for confirming that a TSP meets the requirements for issuing qualified certificates under Regulation (EU) N° 910/2014 [i.1]. NOTE - See ETSI EN 319 403 [i.6] for guidance on assessment of TSP processes and services.

Obsah

ČSN EN 16713-2 This European Standard specifies requirements and test methods for circulation systems and is applicable to equipment used in domestic swimming pools and designed for the circulation of water (introduction and/or extraction). This standard applies for swimming pools as defined in EN 16582-1 and will be read in conjunction with it. This standard does not apply to: - pools for public use covered by EN 15288-1; - spas for domestic or public use; - paddling pools according to EN 71-8; - pre filtration; - natural and nature like pools. NOTE - For filtration systems see EN 16713-1 and for treatment systems EN 16713-3.

Obsah

ČSN EN ISO 28721-5 This part of ISO 28721 establishes a system for the cataloguing of defects in enamellings for chemical service and vessels. In addition, it describes some types of areas in which defects have been treated and which can easily be confounded with enamelling defects. It serves for a consistent language use concerning the designation and characterization of enamelling defects. This part of ISO 28721 is limited to detectable defects and does not purport to fully take into consideration all occurring types of defects. It does not evaluate enamelling defects; the classification carried out is based on experience and corresponds, as far as possible, to ISO 28721-1.

Obsah

ČSN EN ISO 16278 ISO 16278:2016 defines the characteristics required to synthetically describe the organization and content of human anatomy within a terminological system. It is intended primarily for use with computer-based applications such as clinical electronic health records, decision support and for various bio-medical research purposes. ISO 16278:2016 will serve to - facilitate the construction of new terminological systems in a regular form which will increase their coherence and expressiveness, - facilitate maintenance of human anatomy within terminological systems, - increase consistency and coherence of existing terminological system, - allow systematic cross-references between items of human anatomy in different types of ter-minological systems, - facilitate convergence among human anatomy within terminological systems, - make explicit the overlap for human anatomy between different health care domains termino-logical systems, - provide elements for negotiation about integration of different terminological systems into in-formation systems between the respective developers, and - enable the systematic evaluation of human anatomy within terminological systems. ISO 16278:2016 itself is not suitable or intended for use by, individual clinicians or hospital ad-ministrators. The target groups for this International Standard are the following: - designers of specialized standard healthcare terminological categorial structures; - developers of healthcare terminological systems including classifications and coding systems; - producers of services for terminological systems and designers of software including natural language processing; - information modellers, knowledge engineers, and standards developers building models for health information management systems; - developers of information systems that require an explicit representation of healthcare termi-nological systems; - developers of marked-up standards for representation of healthcare documents. ISO 16278:2016 does not include categorial structure that might be necessary for the description of developmental anatomy during the human life cycle, which includes prenatal development, post-natal growth and aging. ISO 16278:2016 has been developed for use as an integrated part of computer-based applications and for the electronic healthcare record. It would be of limited value for manual use. It is not the purpose of this International Standard to standardize the end user classification of human anatomy terminology or to conflict with the concept systems embedded in national practice and languages.

Obsah

ČSN EN ISO 14270 Tato norma stanoví rozměry vzorku a postup pro mechanizované odlupovací zkoušení jednotlivých odporových bodových, švových a výstupkových svarů u přeplátovaných plechů z jakýchkoliv kovových materiálů tloušťky od 0,5 mm do 3 mm, kde svary mají maximální průměr 7 t (kde t je tloušťka plechu v mm). Pokud se používají doporučené rozměry zkušebního vzorku, pak u svarů o průměru 5 t a 7 t je možné odhadnout sílu pro odloupnutí příliš nízkou. Účelem mechanizovaného odlupovacího zkoušení je stanovení síly pro odloupnutí, kterou může zkušební vzorek vydržet.

Obsah

ČSN EN 62779-1 Norma definuje obecné požadavky na polovodičové rozhraní, které se používá pro komunikaci s lidským tělem (HBC). Jsou zde zahrnuty obecné a funkční specifikace rozhraní stejně jako limitní a provozní podmínky. Norma obsahuje informativní přílohu A, která uvádí obecný popis HBC, informativní přílohu B, která obsahuje vytváření výkonného šumového signálu v HBC a informativní přílohu C, kde je uveden výpočet meze citlivosti.

Obsah

ČSN EN 60958-4-4 Tato norma specifikuje fyzikální a elektrické parametry pro různá média. Spolu s IEC 60958-1, IEC 60958-4-1 a IEC 60958-4-2 specifikuje rozhraní pro sériový digitální přenos ze dvou kanálů, ze kterých jsou periodicky odebírány vzorky a lineárně zastoupeny digitální zvuková data z jednoho vysílače do jednoho přijímače.

Obsah

ČSN EN 60958-4-2 Tato norma specifikuje formát pro kódování metadat a subkódů, které se vztahují k zvukovému obsahu a jsou s ním přenášeny. Spolu s IEC 60958-1, IEC 60958-4-1 a IEC 60958-4-4 specifikuje rozhraní pro sériový digitální přenos dvou kanálů, ze kterých jsou periodicky odebírány vzorky a lineárně zastoupeny digitální zvuková data z jednoho vysílače do jednoho přijímače.

Obsah

ČSN CLC/TS 50612 Tato norma uvádí návod pro výběr, použití a údržbu přenosných elektrických zařízení, která splňují EN 50379-1 4 a EN 50379-2 5 nebo EN 50379-3 6 a jsou navržena pro měření parametrů spalinových plynů u ústředních vytápěných bojlerů, které používají první, druhé nebo třetí plyny pro domácnosti podle následujícího popisu: 1) plynové spotřebiče typu A, B a C, kromě těch spotřebičů, kde předpisy (viz 7.3.2.1), zakazují vzorky spalování, 2) všechny spotřebiče na plynná paliva, pro které výrobce spotřebiče poskytuje účelově navržené vzorky spalování nebo konkrétní pokyny pro odběr vzorků, jako diagnostický nástroj pomáhající technikům pro: a) potvrzení vyhovujícího spalování v okamžiku uvádění do provozu, v souladu s návody ke spotřebiči nebo národními nebo místními předpisy nebo normami; b) potvrzení vyhovujícího spalování v okamžiku provádění servisu s národními nebo místními předpisy nebo normami nebo po servisu v souladu s návody ke spotřebiči; c) potvrzení vyhovujícího spalování po údržbě, v souladu s návody ke spotřebiči nebo národními nebo místními předpisy nebo normami.

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ČSN EN ISO 16641 This International Standard covers integrated measurement techniques for radon-220 with passive sampling only. It provides information on measuring the average activity concentration of radon-220 in the air, based on easy-to-use and low-cost passive sampling, and the conditions of use for the measuring devices. This International Standard covers samples taken without interruption over periods varying from a few months to one year. This type of measurement is also applicable for determination of radon-222 activity concentration.

Obsah

ČSN EN ISO 18744 This International Standard specifies a method that is applicable for the detection and enumeration of Cryptosporidium oocysts and Giardia cysts on or in food products that are described herein as fresh leafy green vegetables and berry fruits. With suitable controls, it may also be applicable for the examination of other fresh produce. The microscopy descriptions are for Cryptosporidium spp. oocysts and Giardia duodenalis cysts of size ranges which include those species (Cryptosporidium) or assemblages (Giardia) known to be pathogenic to humans. This method does not include any molecular analysis and therefore is not suitable for the determination of the species or genotypes/assemblages of Cryptosporidium oocysts and Giardia cysts. The method will detect all species and genotypes/assemblages that are known to be pathogenic for humans and also others that are not. For further identification, molecular typing assays are required. However, these cannot be reliably performed if process positive controls have been spiked into the samples, as the result of molecular typing assays will be obfuscated. This method does not allow the determination of viability or infectivity of any Cryptosporidium oocysts and Giardia cysts which may be present.

Obsah

ČSN EN ISO 16773-2 This part of ISO 16773 gives guidelines for optimizing the collection of EIS data with focus on high-impedance systems. High impedance in the context of intact coatings refers to systems with an impedance greater than 109 Ohm cm2. This does not preclude measurements on systems with lower impedance. For uncoated samples extra information can be found in ISO/TR 16208. This part of ISO 16773 deals with the following: - instrumental set-up: requirements and pit-falls; - data validation: checking the measurement range and the accuracy of the data; - performing an EIS measurement: specimen considerations and instrumental parameters; - the experimental results: different methods of presenting EIS data. These guidelines are intended to ensure the acquisition of EIS data that can be used to study the performance of the specimen. This part of ISO 16773 does not give guidelines for the interpretation of the data.