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This document specifies general requirements for proficiency tests that are offered to in vivo bioassay measurement facilities operating a whole-body counter (WBC) or partial body counter (PBC) for monitoring of persons. It specifies minimum requirements for proficiency testing applicable to dosimetry laboratories that have dedicated facilities for in vivo monitoring and where accreditation is…

IEC 60115-2-10:2023(E) is a detail specification which specifies the characteristics and ratings of low-power film resistors with leads for use in electronic equipment, which are typically assembled in through-hole technology (THT) on circuit boards. This detail specification establishes test schedules and performance requirements permitting the quality assessment of the resistors covered herein…

IEC 61291-2:2023 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition. IEC 61292-2:2023 provides a performance specification template applicable to optical amplifiers (OAs) used in single…

IEC 61292-2:2023 provides a performance specification template applicable to optical amplifiers (OAs) used in single channel applications. Multichannel applications are covered in IEC 61291-4. The objective of this template is to provide a framework for the preparation of performance standards and/or product specifications defining the performance of OA devices used in single channel applications…

1 Scope This document defines the construction, safety, and performance requirements of modular or factorymatched hydrogen gas generation appliances, herein referred to as hydrogen generators, using electrochemical reactions to electrolyse water to produce hydrogen. This document is applicable to hydrogen generators that use the following types of ion transport medium: — group of aqueous…

1 Scope 1.1 General This Standard is intended to form the basis of a QMS within a health care or home setting for the purpose of providing safe, reliable kidney dialysis treatments. Note: A comprehensive QMS can be achieved when this Standard is used in combination with the following related Standards: a) CAN/CSA-C22.2 No. 60601-1; b) CAN/CSA-C22.2 No. 60601-2-16; c) CAN/CSA-C22.2 No.…

This document specifies the syntax and semantics of COBOL. Its purpose is to promote a high degree of machine independence to permit the use of COBOL on a variety of data processing systems. This document specifies: The form of a compilation group written in COBOL. The effect of compiling a compilation group.  The effect of executing run units. The elements of the language for which a conforming…

This document specifies the syntax and semantics of COBOL. Its purpose is to promote a high degree of machine independence to permit the use of COBOL on a variety of data processing systems. This document specifies: The form of a compilation group written in COBOL. The effect of compiling a compilation group. The effect of executing run units. The elements of the language for which a conforming…

1 Scope 1.1 Standard addresses This Standard is intended to address the safe, effective, and reliable reprocessing of reusable medical devices at each phase of the reprocessing workflow, including a) establishing a QMS for the MDRA, including i) key performance indicators; ii) policies and procedures; iii) documentation; iv) roles and responsibilities; v) management review; vi) planning…

This Standard specifies minimum requirements for zero-copy integration and includes a set of guidelines for building modular capabilities within a controlled data management environment which can be applied either as stand-alone experiences or combined into advanced solutions. This Standard provides a blueprint for IT and other leaders who rely on organizational data integrity to perform…