1326-1350 of 1358 Resource Library
1326-1350 of 1358 Resource Library
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 …
INFOGRAPHIC
Water, water, everywhere, and every drop tested via a mass spectrometer. Such is the dream of many a water analyst. Why such zeal? Because the number of potential water contaminants is growing by the year, and water analysis is the f irst line of defense …
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 …
WEBINAR
High performance FT-IR measurements in all three ranges (mid, near, and far) of the infrared spectrum through a single instrument present possibilities for analysis in a wide range of applications. Watch this webinar to learn how the innovative …
APPLICATION BRIEF
Introduction Glucocorticoid steroids work by suppressing various aspects of the human immune system in conditions where hyperactivity can cause poor health through allergies, inflammation, and autoimmune dysfunction. Betamethasone dipropionate belongs …
APPLICATION BRIEF
Introduction Finasteride is an antiandrogenic compound or ‘testosterone blocker’ which is used as a treatment for an enlarged prostate and can treat male hair loss. It inhibits the production of the enzyme Type-II 5a-reductase which converts …
TECHNICAL NOTE
Page 1 of 3 D-6610 21 CFR Part 11 Pyris Enhanced Security Electronic Records – System Design CFR Ref. Question Pyris Enhanced Security 11.10(a) Does the supplier have a QMS? ISO 9001 11.10(a) Is it possible to see on the system whether or not records have …
APPLICATION BRIEF
Introduction Lamotrigine is an antiepileptic drug in the phenyl triazine class used in the treatment of both epilepsy and as a mood stabilizer for bipolar disorder. It is the first medication since lithium to be granted US FDA approval for maintenance …
APPLICATION BRIEF
Introduction Levetiracetam was approved for medical use in the United States in 1999 and is available as a generic medication. Levetiracetam is a novel anticonvulsant agent used as an adjunct medication to manage partial-onset, myoclonic, and …