In a recent editorial published in Current Pharmaceutical Analysis (Volume 18, Issue 6, 2022), researchers Dr. Behrouz Seyfinejad and Dr. Abolghasem Jouyban highlight the importance of method ...

Producing cGMP biopharmaceutical products requires controlled, consistent performance of the manufacturing process. cGMP also requires controlled, consistent performance of analytical test methods.

This course will provide you with the requisite scientific knowledge and understanding of analytical method lifecycle management, which includes the activities of validation, verification, transfer, ...

Chinese researchers have established CAS(ME) 3, a large-scale, spontaneous micro-expression database with depth information and high ecological validity. It is expected to lead the next generation of ...

Double-data-rate synchronous dynamic random access memory (DDR SDRAM) physical-layer testing is a crucial step in making sure devices comply with the JEDEC specification. The ultimate goal is to ...

Laboratory-based design verification testing (DVT) of combination products and medical devices must be performed to demonstrate that the device meets the performance requirements that were set in the ...

Nonclinical Dose Formulation Analysis Method Validation and Sample Analysis, addresses the fact that no regulatory guidances exist for either nonclincal dose formulation analysis (NCDFA) or for sample ...

As high-throughput genomic sequencing generates increasing data volumes, researchers face challenges in identifying functional gene regions within DNA ...