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API BIOLOGICAL TREATMENT - BIOLOGICAL TREATMENT OF PETROLEUM REFINERY WASTES
January 1, 1963 - API

FOREWORD Increased emphasis on water resources and on water conservation has had a direct effect on the petroleum industry as well as on all other industries which require large volumes of water in their operations. The petroleum industry has become extremely water conscious because in some areas...

SEMI MATERIALS - MATERIALS
SEMI
A description is not available for this item.
ASTM BIOLOGICAL EFFECTS - BIOLOGICAL EFFECTS AND ENVIRONMENTAL FATE
ASTM
A description is not available for this item.
JIS INTERNATIONAL STD - JIS International Standardization Handbook
January 1, 2019 - JSA
A description is not available for this item.
ISO DIS 35001 - Biorisk management for laboratories and other related organisations
August 1, 2018 - ISO

This International Standard defines a process to identify, assess, control, and monitor the risks associated with hazardous biological materials. This International Standard is applicable to any laboratory or other organisation that works with, stores, transports, and/or...

ASTM E2805 - Standard Practice for Measurement of the Biological Activity of Ricin
December 1, 2018 - ASTM

This guide is intended for the manufacturers and users of ricin reference material. Ricin reference materials are well-characterized materials that can be used to test detection devices and calibrate laboratory measurements. It is anticipated that ricin reference...

DS/ISO/TS 20399-3 - Biotechnology – Ancillary materials present during the production of cellular therapeutic products – Part 3: Best practice guidance for ancillary material users
December 10, 2018 - DS

This document provides guidance for ancillary material (AM) users. It is applicable to cellular therapeutic products, including those gene therapy products whereby cells form part of the final product. It does not apply to products without cells. This document focuses primarily on ancillary...

DS/ISO/TS 20399-2 - Biotechnology – Ancillary materials present during the production of cellular therapeutic products – Part 2: Best practice guidance for ancillary material suppliers
December 10, 2018 - DS

This document provides guidance for ancillary material (AM) suppliers to maintain a high level of lot-to-lot consistency in the aspects of identity, purity, stability, biosafety, performance, as well as the accompanying documentation. This document is applicable to cellular therapeutic...

ISO TS 20399-3 - Biotechnology - Ancillary materials present during the production of cellular therapeutic products - Part 3: Best practice guidance for ancillary material users
November 1, 2018 - ISO

This document provides guidance for ancillary material (AM) users. It is applicable to cellular therapeutic products, including those gene therapy products whereby cells form part of the final product. It does not apply to products without cells. This document focuses primarily on ancillary...

ISO TS 20399-2 - Biotechnology - Ancillary materials present during the production of cellular therapeutic products - Part 2: Best practice guidance for ancillary material suppliers
November 1, 2018 - ISO

This document provides guidance for ancillary material (AM) suppliers to maintain a high level of lot-to-lot consistency in the aspects of identity, purity, stability, biosafety, performance, as well as the accompanying documentation. This document is applicable to cellular therapeutic...

ASTM F2038 - Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part I—Formulations and Uncured Materials
December 1, 2018 - ASTM

This guide is intended to educate potential users of silicone elastomers, gels, and foams relative to their formulation and use. It does not provide information relative to silicone powders, fluids, or other silicones. The information provided is offered to guide users in the selection of...

ISO DIS 20579-3 - Surface chemical analysis - Sample handling, preparation and mounting - Part 3: Biomaterials
November 5, 2018 - ISO

This part 3 of the International Standard gives guidance on methods of handling, mounting and surface treatment for a biomaterial specimen prior to surface chemical analysis. It is intended for the analyst as an aid in understanding the specialized specimen-handling conditions required for...

ISO DIS 5840-2 - Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes
January 14, 2019 - ISO

This part of ISO 5840 is applicable to heart valve substitutes intended for implantation in human hearts, generally requiring cardiopulmonary bypass and generally with direct visualization. See Annex E for examples of surgical heart valve substitutes and their components. This part of ISO 5840 is...

DS/ISO 20387 - Biotechnology – Biobanking – General requirements for biobanking
August 6, 2018 - DS

This document specifies general requirements for the competence, impartiality and consistent operation of biobanks including quality control requirements to ensure biological material and data collections of appropriate quality. This document is applicable to all organizations...

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