04.11.26 -- Pharmaceutical Online Best Of March

Join Pharmaceutical Online Chief Editor Katie Anderson and experts for this virtual event, Proactive Contamination Control in Aseptic Fill/Finish. They will explore topics such as risk-based facility and equipment design, advanced barrier technologies, personnel and material flow optimization, environmental monitoring trending and data analytics, and the integration of rapid microbiological methods. Registration is free!

For those involved in outsourcing, the new FDA draft guidance regarding FDA Form 483 observations reshapes the accountability framework. The public comment period ends May 8.

A new draft guidance document from ICH, issued jointly with the EMA, adopts the position that the assessment of leachables and extractables requires a holistic framework for risk evaluation.

Fill/finish operations are famously resource heavy. Nonetheless, Novo set out to achieve ambitious environmental goals with its $4.1 billion project in North Carolina.

Identifying process redundancies and enhancing visual management allows manufacturers to stabilize workflows. These data-driven improvements can decrease operational variability by nearly 50%.

Master the complexities of modern sterility assurance. Explore expert guidance on risk-based planning and automated integration to ensure your new filling line meets the highest standards.

New materials, smart automation, and in-press quality control are optimizing tablet compression. These five key innovations are driving efficiency and consistency in solid dose manufacturing today.