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Pharmaceutical Testing Articles & Analysis
11 articles found
Abstract In pharmaceutical synthesis, heavy metal catalysts are commonly used, and their residues often remain in the final product. ...
In the realm of pharmaceutical research and development, ADME testing services play a pivotal role in evaluating the pharmacokinetics of drug candidates. ...
This article delves into the nuances of CGMP manufacturing, including pilot scale-up and commercial manufacturing aspects, along with the facilities and services that support these crucial processes. What is Pharmaceutical CGMP Manufacturing? Pharmaceutical CGMP manufacturing refers to producing pharmaceutical products under regulatory ...
Drug analysis refers to the detection and analysis of ingredients and contents in drugs. Drug analysis and testing involves the study of composition, physical and chemical properties, purity, and the determination of the content of active pharmaceutical ingredients and their preparations, to ensure that the medications are safe, rational, and effective. Drug ...
Temperature and humidity monitoring play a major role in ensuring safety, quality, and potency in the pharmaceutical processing chain. However, an aspect that is sometimes understated is the importance of continued monitoring during transport and delivery. ...
As part of their pharmaceutical development, Almac use the Gaspace Advance Micro from Systech Illinois to test oxygen levels in pharmaceutical packaging. ...
Fresenius is fast emerging as a leading player in oncology generics on the strength of its comprehensive product portfolio of injectables, oral cytotoxics, cytostatics, intermediates and active pharmaceutical ingredients (APIs). Imran Ahmed, Senior Research Scientist at Fresenius, shared with us how the use of Peak Scientific's generators have provided peace of mind and easier ...
Lots are released based on comparing test results from a sample to lot acceptance procedure criteria. If a set of test results meets the lot acceptance procedure criterion, how can I be assured that another sample from the lot would also pass the criterion? ...
Customer: Butterworth Laboratories, United Kingdom Wilh nearly 40 years' experience, Butterworth Laboratories remains an independent UK con¬tract analytical service providing Method Development, Method Validation, Stability Testing and OC Testing to the pharmaceutical, medical device and chemical industries. ...
ByBUCHI
There are STANDARD Guidelines used to define the Identification and Purity of compounds used in Pharmaceutical and Cosmetic formulations, as well as the final Products. These protocols are described in great detail in the various Monographs of the United States and British Pharmacopoeias, the National Formulary (USP/NF and BP), the International FAO/WHO Codex (CODEX) and other ...
Since the announcement of the birth of Dolly the cloned sheep in February 1997, assiduous attempts have been made to emphasise the potential benefits of human cloning techniques that do not result in a cloned baby: replacement body organs; cancer and ageing research; testing new pharmaceuticals, to name a few. Such research would nonetheless pave the way for the ...