07.11.26 -- Pharmaceutical Online Newsletter - Best Of June

Join Chief Editor Katie Anderson and her expert panel on July 29, 2026 at 11 AM ET. for a special Pharmaceutical Online Live discussion: Building Inspection-Ready Systems with Digital Documentation. The discussion will focus on how digital documentation is reshaping inspection readiness and offer actionable insights on moving from reactive inspection preparation to a sustainable state of continuous readiness through digital transformation. Registration is free thanks to Thermo Fisher Scientific.

How API manufacturers can assess and mitigate organic impurities and nitrosamines using risk-based strategies aligned with global regulatory expectations.

Pharmaceutical continuous manufacturing is an enabler of better manufacturing, but only when implemented with intention.

This is the first published application of data envelopment analysis to six major pharmaceutical analytical validation guidelines, including ICH Q2(R2), USP, ChP, and Brazil's ANVISA.

As portfolios expand, production teams face mounting pressure to move faster. Learn how manufacturers are addressing rising complexity while maintaining performance across operations.

Discover strategies to calibrate testing scope to risk, optimize execution workflows, and reduce operational burdens without compromising quality standards or safety compliance.

Review the crucial selection of the optimal solid form in  carefully achieving successful jet milling of APIs designed specifically for pulmonary administration through the pulmonary route.