Micromeritics Instrument Launches the SAS II for Particle Sizing
The device uses the air permeability technique to enhance the productivity and accuracy of particle sizing.
Micromeritics Instrument, a material characterization technology company based in Norcross, GA, announced the launch of the Sub-Sieve Autosizer II (SAS II), a device that enhances the productivity and accuracy of particle sizing via the air permeability technique, on Dec. 3, 2019.
According to a company press release, the autosizer comes equipped with fully automated measurement sequences which include computer-controlled sample compaction and pressure stability for high repeatability. Reports are generated automatically and can be customized to meet company requirements as security features lock down measurement methods and configuration parameters from unofficial changes.
The device handles particle size measurements from 0.2 µm to 75 µm by using the non-destructive air permeability technique to measure the pressure drop across a packed bed of sample at a defined air flow rate, accurately measuring finer powders, according to the release. Additionally, the autosizer functions with specific ASTM standards including E2980, E2651, B330-12, and B330-15 for metal powders and C721-15 for alumina and silica powders.
Source: Micromeritics Instrument
Why is the PDA Pharmaceutical Microbiology Conference the Hottest Ticket in the Industry?
October 10th 2024Get a glimpse of the power and popularity behind the PDA Pharmaceutical Microbiology Conference from two planning committee members, Julia Marre, PhD (Associate Director, Scientific and Regulatory Affairs at Pocket Naloxone Corp) and Dawn Watson (Executive Director, Global Micro Quality and Sterility Assurance at Merck). This candid conversation reveals why this industry event is so influential…and always sold out! The speakers discuss what makes the PDA Pharmaceutical Microbiology Conference so vital to industry professionals, as well as how to become a part of this dynamic professional community.
Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies
November 21st 2024Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.
Your Ultimate Guide for CMC Testing Support for Gene and Cell Therapy
November 21st 2024Explore the complexities of gene and cell therapy development with our comprehensive guide to Chemistry, Manufacturing, and Controls (CMC) testing. Learn how our expertise ensures the safety, potency, and quality of advanced therapies, supporting your journey from product development through regulatory approval.
