Clinical Research Contamination Life Science Regulation 
Advarra
SEPTEMBER 14, 2023
In the clinical research space, GxP is a set of quality regulations and guidelines designed to establish the safety, efficacy, and integrity of pharmaceuticals, medical devices, and clinical trials. This blog explores key concepts, regulations, and the importance of GxP in delivering successful clinical trials.
Cloudbyz
NOVEMBER 3, 2021
Biosamples and biomarkers are the core basis for much of the work done in the clinical research industry and proficient Human Biosample Management (HBSM) is necessary to procure reliable biosamples. Muscle tissues, nerve tissues, cell lines, blood cells, stem cells, and more. Sample Backup. Let’s use the easiest example of a sample.
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XTalks
NOVEMBER 7, 2022
“Liquid biopsies have demonstrated promising activity in multiple clinical settings, but the great enthusiasm and expectations around them can be harmful if not adequately managed,” said Dr. El Mustapha Bahassi, PhD, Director, Clinical Laboratory Sciences, at the global clinical research organization (CRO) Medpace.
XTalks
SEPTEMBER 14, 2020
Meanwhile, N95 masks are in such short supply that regulators have told healthcare workers they can be used multiple times with little evidence that disinfecting them works. Below are some free webinars you can register for that have delved into the topic: Continuing Clinical Research Innovations After COVID-19.
Drug Discovery World
AUGUST 10, 2022
For example, it is challenging to regulate transgene copy numbers in each T cell, posing safety risks. Although transgenes show a preference for certain sites, the CAR transgene could integrate into the T cell genome at any location, including within a sequence that regulates oncogene expression, thereby increasing cancer risk.
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