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ASTM - ASTM International: Recent submissions
Now showing items 1241-1260 of 39933
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Standard Practice for Quality Control of Routine Testing in a Laboratory
Abstract: 4.1 Test Method Monitoring Program—A testing laboratory conducting a test method on a routine basis should ensure the quality of its test results through a test method monitoring program (TMMP). A TMMP provides repeated ... -
Standard Guide for Odor Evaluation of Absorbent Hygiene Articles
Abstract: 5.1 This guide provides general guidelines and recommendations for evaluating odor of absorbent hygiene articles simulating product experience under controlled conditions. Absorbent hygiene categories include but are not ... -
Standard Guide for Moving Sites to Closure (MStC) for Petroleum Underground Storage Tank (UST) Releases
Abstract: 4.1 This guide is intended for use primarily by responsible parties, corrective action professionals, regulators, and others who desire to secure regulatory closure or an NFA certification from the applicable regulatory ... -
Standard Terminology for Diversity, Equity, and Inclusion (DEI) Needs Assessment
Abstract: 2.1 In the realm of DEI, precise and shared understanding of terminology is foundational to creating a robust needs assessment. 2.2 Terms such as “diversity,” “equity,” and “inclusion” are complex and multifaceted, often ... -
Standard Test Method for Evaluating the Impact of Nanomaterials on Phagocytic Function in Vitro
Abstract: 5.1 This test method evaluates the effects of nanomaterials on the phagocytic function of phagocytic cells. 5.2 This luminol chemiluminescence-based assay is a measure of “phagocytic function,” including the ability to ... -
Standard Guide for Diversity, Equity, and Inclusion (DEI) Needs Assessment
Abstract: 2.1 This guide will encompass: 2.1.1 Core Principles—Guiding principles for conducting a needs assessment with a DEI lens ensuring equity, accessibility, and representation. 2.1.2 Data Collection Methods—Recommended ... -
Standard Guide for Characterization of Encapsulation, Extraction, and Analysis of RNA in Lipid Nanoparticle Formulations for Drug Delivery
Abstract: 5.1 Nucleic acid therapeutics based on the utilization of mRNA or modifications thereof are increasingly important for enabling the production of therapeutic proteins, vaccines, genome editing modalities, etc. To establish ... -
Standard Practice for Determining the Bacterial and Fungal Inhibition of a Vapor Releasing Test Substance Under Simulated Field Conditions
Abstract: 5.1 This practice may be used to determine the effectiveness of continuous active/passive vapor delivery products to inhibit the growth of organisms in areas containing a high level of humidity and a high ambient air ... -
Standard Guide for Using FMECA and HACCP for Performing Risk Identification, Risk Analysis & Risk Control on Cleaning Processes for Pharmaceuticals and Medical Devices
Abstract: 4.1 This standard provides guidance on using failure modes, effects and criticality analysis (FMECA), and hazard analysis and critical control points (HACCP) to perform the risk identification and risk analysis on cleaning ... -
Standard Terminology for Pesticide Application with Drones
Abstract: 3.1 Define and standardize common terms used for application of pesticides by drones. -
Standard Practice for Validation of Test Methods for the Counting and Sizing of Particulate Matter on the Surfaces of Single-Use Bioprocessing Equipment
Abstract: 4.1 In the absence of standards pertaining to the measurement of particulate matter present on the surfaces of SUS, a longstanding practice is to adapt USP <788> (harmonized with Ph. Eur. 2.9.19 and JP 6.07) to SUS. However, ... -
Standard Specification for Nickel-Iron-Chromium-Silicon Alloys Plate, Sheet, and Strip
Abstract: This specification covers nickel-iron-chromium-silicon alloys (UNS N08330 and N08332) plate, sheet, and strip intended for heat resisting applications and general corrosive service. The alloy UNS N08830 and UNS N08332 shall ... -
Standard Guide for Development of Test Methods for the Counting and Sizing of Particulate Matter on the Surfaces of Single-Use Bioprocessing Equipment
Abstract: 4.1 In the absence of standards pertaining to the measurement of particulate matter present on the surfaces of SUS, a longstanding practice is to adapt USP <788> (harmonized with Ph. Eur. 2.9.19 and JP 6.07) to SUS. However, ... -
Standard Practice for Evaluating DICONDE Interoperability for Image and Presentation State Display
Abstract: 5.1 This practice describes the recommended procedure for NDE system manufacturers and NDE system purchasers to assess a system’s level of compliance and conformance to the DICONDE standard related to image and presentation ... -
Standard Guide for Principles of Circular Product Design
Abstract: 5.1 In a circular economy, products and their materials can maintain economic and societal value through resource management actions such as: (1) extended-use processing strategies, including reuse, repair, retrofit, and ... -
Standard Guide for Interpretation and Reporting in Forensic Comparisons of Trace Materials
Abstract: 5.1 This guide focuses on a qualitative approach to communicate the significance of an association or exclusion, based on (1) the validated methodology used for the comparison of the items, (2) discrimination capabilities ... -
Standard Guide for PFAS Data Evaluation
Abstract: 4.1 This guide can be used before data are collected for a PFAS sampling project to aid in planning the analysis and selecting the laboratory. 4.2 The users of this guide should consider assembling a team of experienced ... -
Standard Practice for On-Site Identification of Firestop Systems and Judgments
Abstract: 4.1 This practice is important because it will help the inspector to understand who performed the firestopping, when the firestopping was installed, and the method utilized to perform the firestopping so that it can be ... -
Standard Practice for Testing Antimicrobial or Disinfectant Efficacy Against Biofilms Grown on a Medical Device or Surface by the Biofilm Surface Test Protocol (BSTP)
Abstract: 5.1 Vegetative biofilm bacteria are phenotypically different from suspended planktonic cells of the same genotype (9). Biofilm is the etiological agent of many implant and device-related infections and, once established, ... -
Standard Guide for Development and Validation Considerations of Advanced Process Control (APC) in Commercial Pharmaceutical Manufacturing
Abstract: 5.1 APC is the foundation to smart manufacturing. Smart manufacturing has emerged as one key concept as the industry transitions to an Industry 4.0 paradigm. FDA has also recognized this industry trend and published a ...