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601-625 of 1418 Resource Library
601-625 of 1418 Resource Library
WHITE PAPER
    Introduction Data integrity compliance has become a large and crucial part of drug manufacturing operations. Here, we review the data integrity and CSV regulatory setting in the United States (US) and the European Union (EU), discuss some of the …
WHITE PAPER
    Introduction This white paper is designed to provide an overview of the evolving regulations as laid out in the proposed new EU drinking water standards. It offers a summary of the standards and targeted analytes covered under the 2020 EU provisional …
APPLICATION BRIEF
  Introduction Epoxy resins are important CASE (coatings, adhesives, sealants, elastomers) materials for industrial and consumer applications due to their versatility. Epoxy resins can be designed as adhesives or for coatings, they can be formulated to …
WHITE PAPER
  Introduction Microplastics are becoming a major global environmental concern with plastics and microplastics turning up in everything and everywhere - including consumer products, especially food and beverages, and even within the digestive systems of …
WEBINAR
Introduction Professor Denise Mitrano of ETHZurich provides an overview of her recent research on the effectiveness of technical water systems such as wastewater and drinking water treatment plants at removing nanoplastics and microplastics from water. …
APPLICATION BRIEF
  Introduction Near infrared reflectance (NIR) is an excellent method to test feather meal samples for nutritional composition. The DA 7250 performs multi-component analysis for moisture, protein, fat, and ash in less than 10 seconds. … Analysis of …
APPLICATION BRIEF
  Introduction This Application Brief demonstrates the ability of PerkinElmer's LC 300 instrument platform, and SimplicityChrom ™ chromatographic data system (CDS) software to successfully meet the United States Pharmacopeia (USP) performance requirements …
WHITE PAPER
    Introduction The screen or paper on which you are reading this, your chair, the way your drinking water is pre-treated, the pain reliever you reach for – all these diverse items and processes rely on the chemicals industry. The global chemicals …
WHITE PAPER
    Introduction The FDA defines data integrity as “completeness, consistency, and accuracy of data. Complete, consistent, and accurate data should be attributable, legible, contemporaneously recorded, original or a true copy, and accurate (ALCOA)”. ALCOA …
WHITE PAPER
    Introduction Connectivity is happening now, touching many essential parts of our lives—from the “smart” mobile phones we use to the servers where our data is stored. Additionally, routine signals are part of our daily routines—everything from the …
WHITE PAPER
    Introduction Based on EPA modeling, Method EPA 325 A/B will lead to a reduction of an estimated 52,000 tons per year of volatile organic compounds being emitted into the environment. In the face of this major new environmental standard, we can all …
WHITE PAPER
    Introduction The potential of all solid-state battery (ASSB) technology to revolutionize the battery industry is resulting in new battery designs and material configuration solutions. These advancements will unlock chemistry limitations from …
WHITE PAPER
    Introduction This white paper discusses what testing is required at each step in the polymer production lifecycle from R&D to manufacture to recycling. It explores the analytical technologies that will meet those testing needs, and important …
WHITE PAPER
    Introduction One of the goals of QbD is to ensure that all sources of variability affecting a process are identified, explained, and managed by appropriate measures so that the finished medicine consistently meets its predefined characteristics from …
WHITE PAPER
    Introduction In the pharmaceutical manufacturing field, it is critical that computerized systems comply with the U.S. FDA’s 21 CFR Part 11 and EU Annex 11 regulations to ensure data accuracy, integrity and reliability, and sample preparation is no …
WEBINAR
The proposed European Union provisions for safe and clean drinking water include substantial revisions to existing drinking water standards. These represent some of the most extensive requirements affecting the drinking water industry ecosystem, including …
WHITE PAPER
    Introduction Per- and polyfluoroalkyl substances (PFAS) have gained significant attention as an emerging environmental and safety threat in the United States. Since the 1940s, PFAS are ubiquitous in industrial usage due to their chemical stability, …
WHITE PAPER
    Introduction Extractables and leachables studies are critical for maintaining the quality of your drug product and complying with GMP regulations during drug development and final batch release. Exposure to extractables and leachables could have a …
WHITE PAPER
    Introduction One of the biggest fears of any laboratory manager, research scientist, or instrument technician is the thought that dirty power may be affecting their ability to effectively operate critical analytical instrumentation. Dirty power causes …
WHITE PAPER
    Introduction Manufacturers of generics and biosimilars must adhere to stringent quality, safety, and efficacy requirements during drug development; however, there are key differences between the two. “Generic products must demonstrate bioequivalence …
WHITE PAPER
    Introduction In a recent interview with Dr. Mansoor Amiji, University Distinguished Professor, Professor of Pharmaceutical Sciences and Professor of Chemical Engineering at Northeastern University, Boston, MA, USA, we explored the guidelines that …
TECHNICAL NOTE
    Introduction PerkinElmer's Avio ® Max series ICP-OES spectrometers feature a free-running solid-state RF generator for Flat Plate ™ plasma, a proprietary technology which generates a transversely symmetrical plasma, replacing previous helical-coil …
APPLICATION BRIEF
  Introduction This Application Brief demonstrates the ability of PerkinElmer's LC 300 instrument platform, and SimplicityChrom ™ chromatographic data system (CDS) software to successfully meet the United States Pharmacopeia (USP) performance requirements …
APPLICATION BRIEF
  Introduction This Application Brief demonstrates the ability of PerkinElmer's LC 300 instrument platform, and SimplicityChrom ™ chromatographic data system (CDS) software to successfully meet the United States Pharmacopeia (USP) performance requirements …
TECHNICAL NOTE
    Introduction Over the years, many types of analytical instruments have been reduced to a portable or hand-held format to be used in the field, including XRF, LIBS, Raman, FT-IR and NIR analyzers. However, shrinking a gas chromatograph/mass …