Rubber and latices — Nomenclature
Rubber and latices — Nomenclature

Natural gas — Determination of sulfur compounds — Determination of hydrogen sulfide content by UV absorption method
Natural gas — Determination of sulfur compounds — Determination of hydrogen sulfide content by UV absorption method

Anti-bribery management systems — Requirements with guidance for use
Anti-bribery management systems — Requirements with guidance for use

Information security, cybersecurity and privacy protection - Guidelines on personally identifiable information deletion (ISO/IEC 27555:2021)
The standard contains guidelines for developing and establishing policies and procedures for deletion of PII in organizations by specifying: — a harmonized terminology for PII deletion; — an approach for defining deletion rules in an efficient way; — a description of required documentation; and — a broad definition of roles, responsibilities and processes. This document is intended to be used by organizations where PII are stored or processed. This document does not address: — specific legal provision, as given by national law or specified in contracts; — specific deletion rules for particular clusters of PII as are to be defined by PII controllers for — processing PII; — deletion mechanisms; — reliability, security and suitability of deletion mechanisms; — specific techniques for de-identification of data.

Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques - Amendment 1 (ISO 5840-3:2021/Amd 1:2025)

Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements - Amendment 1 (ISO 5840-1:2021/Amd 1:2025)

Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes - Amendment 1 (ISO 5840-2:2021/Amd 1:2025)

Assistive products for walking manipulated by both arms - Requirements and test methods - Part 2: Rollators - Amendment 1: Removal of brake requirements (ISO 11199 2:2021/Amd 1:2024)
This document specifies requirements and test methods of rollators being used as assistive products for walking with wheels, manipulated by both arms, without accessories, unless specified in the particular test procedure. This document also gives requirements relating to safety, ergonomics, performance and information supplied by the manufacturer including marking and labelling. The requirements and tests are based on every-day use of rollators as assistive products for walking for a maximum user mass as specified by the manufacturer. This document includes rollators specified for a user mass of no less than 35 kg. This document is not applicable to rollators with horizontal forearm supports, classified as walking tables, for which ISO 11199-3 is applicable.

Medical laboratories - Concepts and specifications for the design, development, implementation, and use of laboratory-developed tests (ISO 5649:2024)
This document establishes requirements for assuring quality, safety, performance and documentation of laboratory-developed tests (LDTs) as per their intended use for the diagnosis, prognosis, monitoring, prevention or treatment of medical conditions. It outlines the general principles and assessment criteria by which an LDT shall be designed, developed, characterized, manufactured, validated (analytically and clinically) and monitored for internal use by medical laboratories. The scope includes regulatory authority approved IVD medical devices that are used in a manner differing from approved labelling or instructions for use for that device (e.g. use of a sample type not included in the intended use, use of instruments or reagents not included in the labelling). While this document follows a current best practice and state-of-the art approach, it does not provide specific details on how to achieve these requirements within specific disciplines of the medical laboratory nor specific technology platforms. This document does not specify requirements for examination procedures developed