FDA and EMA have issued 10 guiding principles for AI in drug development with the intended goal of ensuring safety and ...

Chitiz Tayal's metadata tool transforms vendor onboarding in pharmaceutical campaigns, reducing setup times from months to ...

This Auditing for GMP course is specifically designed to address the challenges of GMP auditing for the pharmaceutical industry and present the basic competencies required to effe ...

TRS offers a robust solution for analyzing heterogeneous samples, providing comprehensive spectral data essential for ...

As drug development becomes more complex, so do the demands for accurate, reproducible bioanalytical data to prove their safety and efficacy. Method validation ensures the reliability of ...

A new consensus document developed by The Blood Profiling Atlas in Cancer (BLOODPAC) Consortium was published in JCO ...

AI and machine learning are revolutionizing drug discovery, development, and lifecycle management, addressing industry ...

Converge Bio, the AI platform for accelerated drug discovery and development, announced today $25 million in Series A funding, bringing its total raised to $30 million. The round was led by Bessemer ...

The attributes of the DS or DP that are to be tested to obtain the necessary information about product quality safety and efficacy are determined during the Drug Development stage. The information ...

Gene that drops early in pancreatic tumors linked to shorter survival at stage II. Findings could guide future treatment ...

Published in JCO Precision Oncology, the new analytical validation standards offer an industry-wide protocol for test developersCHICAGO, Jan. 15, 2026 /PRNewswire/ -- A new consensus document ...

Sterilization services are growing due to regulatory demands and quality standards. Key opportunities include adopting innovative technologies, forming strategic partnerships, and offering flexible ...