In my May 2020 CW column, I introduced a new test method for measuring the fracture toughness within the facesheet-to-core interface region of sandwich composites. This proposed test method, referred ...
In this chapter, we focus on two topics: the lack of enforcement of existing U.S. Department of Defense (DOD) guidelines and procedures and the role of the program manager in the acquisition process.
Alternative methods to the use of animals in pharmaceutical testing are becoming more used and accepted. Laura Lotfi of ...
Company secures $5M in funding to accelerate its rapid testing platformUSP<1223> Validation achieved, reinforcing 20-hour testing ...
Safety and efficacy are the two regulatory benchmarks for pharmaceutical products. Microbial contamination of products is an important aspect of product quality that can affect both safety and ...
The use of simulation for product development a virtual test environment is becoming increasingly common. Punch Powertrain applies a range of simulation tools which can augment traditional physical ...
Unlock the full InfoQ experience by logging in! Stay updated with your favorite authors and topics, engage with content, and download exclusive resources. Dany Lepage discusses the architectural ...
Manual testing seems cheaper but slows releases, increases risk, and wastes talent. Learn why leaders are shifting to ...
This appendix presents a brief overview of the defense acquisition process. 1 The diagram below from the U.S. Department of Defense (2008:12 enclosure 2) depicts the development of defense systems as ...
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