04.12.25 -- Pharmaceutical Online Best Of March

Whether you're breaking ground on a brand-new manufacturing facility or looking to upgrade an existing site, there are a dizzying number of considerations. Join Pharmaceutical Online Live on Wednesday, April 16th for a digital panel discussion on key factors in facility design, from construction sequencing to site validation. Registration is free thanks to the support of AES.

Of the 190 warning letters that the FDA issued to drug and biopharma manufacturers in the fiscal year 2024, delve into a deep dive on trends pertinent to the 111 inspection-based letters.

Examine an overview of market research on GLP-1 drugs in diabetes and obesity treatments, as well as the anticipated growth of the market and the current leaders in the space.

While AI systems offer advanced capabilities for data analysis, process optimization, and quality assessments, your quality team must first be proficient in interacting with them.

Explore the challenges imposed by deep cold storage conditions and outcomes on functional performance, sub-visible particle performance, and container closure integrity related to syringes.

Discover the advantages of Liquid Chromatography-Mass Spectrometry system monitoring software in PFAS analysis, including improvements in resource efficiency and operational performance.

Become equipped with the tools and strategies needed to strengthen your calibration efforts and better position your organization for success in regulatory audits.