Transform the way you think and act with relevant training and education from Prompt Praxis Laboratories.
Lisa McChesney-Harris, PhD
CEO, CSO & Founder
Lisa McChesney-Harris, PhD
CEO, CSO & Founder
Drug diversion testing is a crucial aspect of healthcare that ensures patient safety and the proper use of controlled substances. Drug diversion refers to the illegal transfer of prescription drugs from the legal supply chain to the illegal market.
When it comes to pharmaceuticals, ensuring quality and safety is of paramount importance. One crucial aspect of this process is sterility testing. In this article, we will dive into the intricate details of sterility testing and explore its significance in the pharmaceutical industry.
Regular quality control product testing is a critical aspect of ensuring the overall quality and reliability of products. From electronics to pharmaceuticals, conducting frequent testing helps identify any potential issues or defects early on, preventing costly consequences down the line. But how often should companies perform these tests to strike the right balance between efficiency and effectiveness?
Sterility testing, also known as drug testing, is a process used to detect the presence of drugs, such as cocaine or heroin, in a person’s system. It typically involves providing a urine sample, an oral fluid sample, a blood sample or all three.
At Prompt Praxis Labs, we provide you with the latest and most reliable drug potency testing services. Our laboratory testing is designed to provide an accurate measure of the potency of your drug sample.
Analytical Method Development and Validation (AMV) involves the process of creating and testing new analytical techniques to accurately measure components of products.
Creating unrivaled capacity for timely results.
Prompt Praxis Laboratories, analytical testing labs, provide a full range of rapid testing and support services focusing on pharmaceutical products and compounded sterile or nonsterile preparations.
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Prompt Praxis Laboratories, LLC, founded in 2011, is a women-owned fully-integrated analytical and microbiological testing lab powered with the current information technology to facilitate rapid drug development.
FDA Establishment Identifier:
3009381492
GDUFA Self-Identified
Illinois DEA:
(Analytical Laboratory, Schedules II-V)
097.001930
Federal DEA:
(Analytical Laboratory, Schedules II-V)
RM0458097
Phone
Locations
50 Lakeview Parkway, Suite 123
Vernon Hills, IL 60061-1590
150 N Fairway Drive, Suites 148-154
Vernon Hills, IL 60061-1860
