pharm-stream-recent-webinars
-
Cleanroom Changes In 2026 For Better Contamination Control
12/3/2025
Proactively improve your cleanroom strategy for 2026. Gain actionable insights on leveraging Environmental Monitoring data, optimizing personnel, and managing residue to enhance contamination control.
-
Extrusion-Based ASD Scale-Up: Performance Through Process Understanding
11/20/2025
Explore the formulation and manufacturing considerations for amorphous solid dispersions (ASDs), with a focus on hot melt extrusion (HME) as a scalable and cost-effective technology option.
-
Streamlining pDNA: Capacity, Complexity, And Cutting-Edge Solutions
11/20/2025
Learn how flexible facility design and process innovation are accelerating pDNA manufacturing, as well as key strategies to avoid scale-up pitfalls and meet growing therapeutic demand.
-
EU GMP Annex 11: Compliance Strategy And Digital Solutions
11/18/2025
Explore how EU GMP Annex 11 revisions could reshape global pharmaceutical compliance, as well as strategies for navigating implementation challenges and building future-ready validation programs.
-
Are You Keeping Pace With Oligo Synthesis Optimization?
11/18/2025
The rapidly expanding oligo market demands optimized RNA synthesis. Examine key innovations and workflow insights to maximize resources and control long-term manufacturing costs.
-
From Readiness To Results: Unlocking Capacity For Expanding Product Demand
11/18/2025
Learn the six pillars that bridge operational readiness and operational excellence. Discover a proven framework to build a resilient, high-performing manufacturing operation and unlock necessary capacity.
-
Advancing Topical Formulations With Innovative Preclinical Models
11/17/2025
A robust formulation development approach integrates scientific principles, systematic formulation development, and preclinical models to facilitate early identification of candidates with poor developability.
-
Accelerate Your pDNA And mRNA Process Development
11/13/2025
Explore a structured approach to optimizing and scaling plasmid DNA production using E. coli, with insights into key growth parameters, benchtop feasibility, and pilot-scale performance.
-
Driving Robust Tech Transfer In Biologics: Computational Fluid Dynamics (CFD) Simulation
11/12/2025
Computational Fluid Dynamics simulation is essential for robust biologics tech transfer. See how this predictive tool optimizes critical scale-up processes, reducing risk and expediting time to market.
-
Practical Solutions For Protein Analytics And Residual DNA Testing
11/12/2025
Discover practical solutions for common quality control bottlenecks in biotherapy manufacturing. Learn how to improve protein analytics and DNA testing robustness and accelerate time to market.