Pharmaceutical Microbiology Testing Articles & Analysis
7 articles found
Abstract In pharmaceutical synthesis, heavy metal catalysts are commonly used, and their residues often remain in the final product. These heavy metals—primarily from catalyst residues—not only affect drug efficacy but also pose serious health risks to patients. As a result, pharmacopoeias in various countries impose strict limits on heavy metal content in pharmaceutical substances. ...
Weiss Technik provides cold chain testing chambers and solutions for the transport of vaccines and other temperature sensitive pharmaceutical products. Our test chambers are used to simulate temperatures that products and packaging may encounter during distribution. Cold chain testing refers to a temperature-controlled supply chain for the storage and distribution of products where specific ...
As part of their pharmaceutical development, Almac use the Gaspace Advance Micro from Systech Illinois to test oxygen levels in pharmaceutical packaging. The Almac Group was founded by Sir Allen McClay in 2002 with its global headquarters located in Northern Ireland and extensive facilities in the UK, US and Asia Pacific. Almac offer the most comprehensive range of services extending from ...
Name: Imran Ahmed Job Title: Senior Research Scientist Company: Fresenius Kabi Oncology Ltd., Gurgoan, India Imran Ahmed, Senior Research Scientist, Fresenius Kabi Oncology Ltd Fresenius Kabi Oncology, performing with Precision Fresenius Kabi Oncology Ltd. primarily operates in the field of research and development, as well as manufacturing, of world-class oncology drugs. The company aims ...
Providing Statistical Confidence to Pass Q. 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? A: Companies use lot acceptance procedures to release a lot. Test results from a sample are ...
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 Regulatory ...
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 replication of humans and for ...