SFS Suomen Standardit

 

This document specifies general requirements for the provision of interpreting services. Additionally, it provides recommendations of good practice. In this document, interpreting refers to the activity performed by human beings to convey spoken or signed content from one language to another. AI-driven interpreting is outside the scope of this document.

 

This International Standard specifies the requirements for performance, sizing, marking and test methods for deck safety harnesses and safety lines on recreational craft. It is applicable to harnesses and lines in the following sizes of body mass: which are intended to be worn by all persons when in the exposed cockpit or on the working deck of a craft afloat. It is not applicable to dinghy “trapeze” harnesses, windsurfing harnesses, seat harnesses for fast motor boats, and harnesses intended to protect against falls from a height.

 

This document specifies general characteristics and test methods for determination of volume and carrying capacity of flexible carrier bags with handles for transport of various unspecified retail goods. This document is applicable to: - carrier bags made of paper, thermoplastic material and/or any other flexible material; - carrier bags with any shape and dimension; - carrier bags with or without gussets.

 

This document specifies the characteristics, qualification and acceptance requirements for bolts with MJ threads in NI-PH2601, passivated, for aerospace applications. Classification: 1 550 MPa1/650 °C. It is applicable whenever referenced.

 

1.1 In scope This document defines a Recommended Practice for Product Structure validation. The objective is to validate the product structure of data ingested, extracted or re-used by the archive. This document defines a method to uniquely identify each node in the product structure and to uniquely define the structure of each assembly node. 1.2 Out of scope This document will not provide validation properties for documents; CAD or other.

 

ISO 12401:2009 specifies the requirements for performance, sizing, marking and test methods for deck safety harnesses and safety lines on recreational craft. It is applicable to harnesses and lines in the following sizes of body mass (multisizing is permitted): size 1: > 50 kg ; size 2: > 20 kg = 50 kg; size 3: = 20 kg; which are intended to be worn by all persons when in the exposed cockpit or on the working deck of a craft afloat. It is not applicable to dinghy 'trapeze' harnesses, windsurfing harnesses, seat harnesses for fast motor boats, and harnesses intended to protect against falls from a height.

 

This document is intended to provide specific levels of information relevant to the identification of a Pharmaceutical Product or groups of Pharmaceutical Products. It defines the data elements, structures and relationships between data elements that are required for the exchange of regulated information, in order to uniquely identify pharmaceutical products. This identification is to be applied throughout the product lifecycle to support pharmacovigilance, regulatory and other activities worldwide. In addition, this document is essential to ensure that pharmaceutical product information is assembled in a structured format with transmission between a diverse set of stakeholders for both regulatory and clinical (e.g. e-prescribing, clinical decision support) purposes. This ensures interoperability and compatibility for both the sender and the recipient. This document is not intended to be a scientific classification for pharmaceutical products. Rather, it is a formal association of particular data elements categorised in prescribed combinations and uniquely identified when levelling degrees of information are incomplete. This allows for Pharmaceutical Products to be unequivocally identified on a global level. References to other normative IDMP standards and specifications for data exchange mechanisms for pharmaceutical product information are included in Clause 2, to be applied in the context of this document. Medicinal products for veterinary use are out of scope of this document.

 

This document specifies a method using light microscopy for the differentiation of the colouration process of fabrics, between dyeing or printing with pigments and, dyeing or printing with dyes. This document is applicable to coloured fabrics with the exception of those made of fibres coloured by melt or dope dyeing.

 

This document specifies an extension of evaluation methods and activities for cryptographic protocols based on ISO/IEC 15408-4 that provides a framework for evaluation methods and activities. This document provides a mapping between the work items for cryptographic protocol evaluation and the associated evaluation activities or evaluation methods. Additionally, this document also provides security assurance classification based on the cryptographic assessment performed by automated provers in four different levels of increasing assurance.

 

This document specifies the requirements for determining fatigue crack growth rates using corner-crack (CC) test pieces. Crack development is measured using a potential-drop system, and the calculated crack depths can be corrected via marker bands created on the fracture surface during the test. Results are expressed in terms of the crack-tip stress-intensity range (?K), with crack depths and test stress level noted.

 

This document specifies safety requirements which need to be observed at design, calculation, manufacture, installation, maintenance, of mobile, temporary installed tents with more than 50 m2 ground area. This document applies also to multiple small tents which are normally not covered by this document and will be installed close together and exceed 50 m2 in sum. NOTE Information is given in Annex C on examination and approval.

 

This document specifies the general characteristics, the conditions for qualification, acceptance and quality assurance, as well as the test programs and groups for non-latching electromagnetic, hermetically sealed relays intended for use in a temperature range from - 55 °C to 125 °C continuous.

 

This document specifies characteristics for 10 A aerospace relays with the following variations of mounting means (e.g. vertical, horizontal), terminal styles (e.g. hooks, pins for soldering, pins for sockets) the associated finishing (e.g. tin plated, gold plated) and coil voltages (e.g. 6 VDC 12 VDC 28 VDC 48 VDC, 115 VAC) for relays with 2, 4 or 6 poles and with or without internal suppressors or LIE protection. The built-in suppressor limits the voltage transients resulting from the electrical power shut off. The relay sockets are not described in this document.

 

This document specifies the test procedures of electromechanical all-or-nothing relays for use in aircraft electrical systems to EN 2282. This document represents the aeronautical version of the standard EN 116000-3 from which it draws inspiration.

 

ISO 11616:2017 is intended to provide specific levels of information relevant to the identification of a Medicinal Product or group of Medicinal Products. It defines the data elements, structures and relationships between data elements that are required for the exchange of regulated information, in order to uniquely identify pharmaceutical products. This identification is to be applied throughout the product lifecycle to support pharmacovigilance, regulatory and other activities worldwide. In addition, ISO 11616:2017 is essential to ensure that pharmaceutical product information is assembled in a structured format with transmission between a diverse set of stakeholders for both regulatory and clinical (e.g. e-prescribing, clinical decision support) purposes. This ensures interoperability and compatibility for both the sender and the recipient. ISO 11616:2017 is not intended to be a scientific classification for pharmaceutical products. Rather, it is a formal association of particular data elements categorised in prescribed combinations and uniquely identified when levelling degrees of information are incomplete. This allows for Medicinal Products to be unequivocally identified on a global level. References to other normative IDMP and messaging standards for pharmaceutical product information are included in Clause 2, to be applied in the context of ISO 11616:2017. Medicinal products for veterinary use are out of scope of ISO 11616:2017.

 

 

This document specifies business requirements for processes intended to preserve digital data. NOTE Data are stored and maintained for the purpose of retrievability and usability during the required archiving period. In addition, for the purpose of some business requirements, data are authentically preserved and accessed. This document is intended to allow for different implementations based on a company’s specific business environment. This document is not intended to incorporate company specific requirements and does not dictate specific organizational structures within a company. This document does not specify a design or an implementation of an archive system. Actual implementations can distribute responsibilities or break out functionality differently. This document assumes that all requirements for configuration management of the product data are in place and therefore are not specifically described in this document.

 

This document specifies a core set of vocabulary, architecture concepts and architecting principles associated with the architecture practice applicable to various entities such as enterprises, business components, capability areas, mission areas, missions, systems, systems of systems, families of systems, infrastructure, products, services, product lines, hardware, software applications and technologies. This document is intended for: This document does not address terms and definitions unique to specific application domains or areas. This document does not address concepts related to architecture competencies.

 

 

This document describes common capabilities, requirements and a supporting information model for logging of events in AI systems. This document is designed to be used with a risk management system.