Мы хотим включить аналитику посещений, чтобы понимать, что искать людям на сайте. Без вашего согласия счётчики не загружаются. Политика конфиденциальности
Найдено: 60+
Overview ISO 8871-3:2003/Amd 1:2018 is an essential international standard concerning elastomeric parts used in parenteral and pharmaceutical devices. This document is an amendment to Part 3 of ISO 8…
Overview ISO 8879:1986/Cor 2:1999 is Technical Corrigendum 2 to the original ISO 8879 standard for the Standard Generalized Markup Language (SGML). Published in 1999, this corrigendum corrects termin…
Overview ISO 8879:1986/Amd 1:1988 is Amendment 1 to ISO 8879:1986 - the international standard for the Standard Generalized Markup Language (SGML). Published by ISO in 1988, this amendment enhances t…
Overview EN ISO 8871-5:2025 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing - is the CEN-adopted version of ISO 8871-5:2025. I…
Overview EN ISO 8872:2022 - titled Aluminium caps and aluminium/plastic caps for infusion bottles and injection vials - General requirements and test methods - is a harmonized European adoption of IS…
Overview EN ISO 8871-2:2020 - "Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization" (ISO 8871-2:2020) specifies procedures for the i…
Overview SIST EN ISO 8871-3:2004/A1:2019 is a European amendment to the international standard ISO 8871-3:2003/Amd 1:2018. It focuses on elastomeric parts used in parenteral and pharmaceutical device…
Overview EN ISO 8871-3:2004/A1:2019 is a European amendment to the international standard ISO 8871-3:2003/Amd 1:2018. It focuses on elastomeric parts used in parenteral and pharmaceutical devices, sp…
Overview ISO 8873-2:2007 - Rigid cellular plastics: Spray-applied polyurethane foam for thermal insulation - Part 2: Application defines requirements for the application and installation of spray-app…
Overview ISO 8873-3:2007 - “Rigid cellular plastics - Spray-applied polyurethane foam for thermal insulation - Part 3: Test methods” defines the laboratory test procedures used to verify spray‑applie…
Overview ISO 8873-1:2006 - "Rigid cellular plastics - Spray-applied polyurethane foam for thermal insulation - Part 1: Material specifications" defines minimum material requirements and test methods…
Overview EN ISO 8871-4:2006 - "Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 4: Biological requirements and test methods" (ISO 8871-4:2006) specifies biological safe…
Overview EN ISO 8871-1:2004 (ISO 8871-1:2003) specifies chemical test methods to classify and evaluate elastomeric parts for parenterals and pharmaceutical devices by determining extractables in aque…
Overview SIST EN ISO 8871-3:2004 is a critical international standard developed by CEN and ISO that specifies methods for evaluating elastomeric parts used in parenteral and pharmaceutical devices. S…
Overview EN ISO 8871-3:2004 is a critical international standard developed by CEN and ISO that specifies methods for evaluating elastomeric parts used in parenteral and pharmaceutical devices. Specif…
Overview EN ISO 887:2000 (ISO 887:2000) - "Plain washers for metric bolts, screws and nuts for general purposes - General plan" - defines the general dimensional system and preferred combinations for…
1 Scope This International Standard specifies the full range of the nominal dimensions of product-grade-A and -C plain washers for general-purpose bolts, screws and nuts of nominal thread diameters r…
What is ISO 8871-2 about? ISO 8871 discusses elastomeric parts for parenterals and for devices for pharmaceutical use. ISO 8871-2 layouts identification and characterization procedures applicable to…
1 Scope This International Standard specifies general requirements and test methods for aluminium caps for injection vials, and for infusion and transfusion bottles.
1 Scope 1.1 This part of ISO 8871 defines procedures for classifying elastomeric parts for primary packs and medical devices used in direct contact with preparations for parenteral use, including bot…
1 Scope This part of ISO 8871 specifies biological requirements for elastomeric parts for parenterals and for devices for pharmaceutical use. It also specifies the test methods, i.e. it offers the ex…
Overview ISO 8871-2:2020 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization - sets out identification and characterization proced…
Overview ISO 8871-1:2003 - “Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 1: Extractables in aqueous autoclavates” defines chemical evaluation procedures for elastom…
Overview ISO 8871-5:2025 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing defines functional requirements and test methods for…
Overview ISO 8870:2006 (IDF 83:2006) - "Milk and milk‑based products - Detection of thermonuclease produced by coagulase‑positive staphylococci" specifies a microbiological method for detecting heat‑…
Overview ISO 8871-3:2003 specifies laboratory methods to determine the number of visible and subvisible particles released from elastomeric parts used with parenterals and pharmaceutical devices. The…
Overview ISO 8872:2022 specifies general requirements and test methods for aluminium caps and aluminium/plastic caps used on infusion bottles and injection vials. This third edition (2022) integrates…
Overview ISO 8879:1986 - Standard Generalized Markup Language (SGML) - is the International Standard for defining and encoding the logical structure of text and office documents. Published by ISO for…