02.10.26 -- New ISPE Framework Targets Uncertainty In Pharma's AI Deployment

Discover the key fabrics used in cleanroom wipes and how they impact performance, as well as substrates, manufacturing methods, and essential attributes to help you choose the right wipe.

Three factors often decide success or failure in FIH studies: integrating biomarkers and pharmacodynamic endpoints, including patients in the trials, and leveraging purpose-built manufacturing.

Rapid growth in cannabinoid and psilocybin therapies demands advanced formulations. Explore capabilities needed to progress from early development through commercial‑ready manufacturing.

Gain insight into how used equipment can deliver faster ROI by eliminating long lead times and reducing capital outlay, allowing for quicker production and revenue generation.

Unlock innovation in biotherapeutics with expert insights into DSC and molecular stability. Learn how biophysical techniques can optimize formulations and enhance nucleic acid stability.

Find out more about the implications of the FDA Modernization Act 2.0, the significance of predictive validity in drug discovery, the efficacy of an innovative human Liver-Chip, and more.

Read about how to overcome tech transfer challenges and ensure consistent content uniformity by leveraging multidisciplinary expertise and decades of commercial encapsulation experience.

Examine strategies to simplify viral vector tech transfers, reduce risk, and maintain quality under tight timelines, as well as a case study that demonstrates how to streamline this critical process.

IoT-enabled smart BMS modernizes cleanrooms through continuous monitoring, predictive analytics, energy efficiency, and strengthened regulatory compliance, enabling more efficient operations.

What if a formulation that removed the need for cold chain distribution was possible? Observe the formulation of vaccines and manufacturing considerations for dry powder inhaled vaccines.

Should you manage certain operations internally or partner with a trusted external provider? Watch experts discuss the benefits of outsourcing stability, storage, and testing.

Biocatalysis delivers cleaner, more selective pharma processes while cutting energy use and waste. Engineered enzymes broaden their reach, enabling faster development and greater sustainability.

Delve into the methods used to evaluate, design, and implement solvent recovery processes, a crucial way to achieve significant reductions in carbon emissions.

Pharmaceutical companies must prioritize patient-centric dosage forms to address challenges like dysphagia, enhance medication compliance, and improve therapeutic outcomes.

Scaling mRNA therapies requires more than innovation—it demands precision. Discover how digital tools like automation and analytics are helping life science companies streamline production.