pharm-stream-recent-webinars

1. How To Address Your Solid Dosage Processing Needs 10/27/2025

   Unlock the keys to consistent solid dosage products. Learn to align unique product needs with optimal processing requirements and equipment strategies. Gain a roadmap for improved quality and reproducibility.

2. Smarter CMC Strategies To Accelerate Next-Gen Biologics To The Clinic 10/23/2025

   Learn how process design and cross-functional collaboration mitigate risks and accelerate the path from early development to FIH manufacturing through real-world case studies of practical approaches.

3. AI In Action: Driving Operational Excellence In Life Sciences 10/20/2025

   Discover how combining domain expertise with advanced AI and data engineering automates compliance, accelerates readiness, and provides real-time insights for confident decision-making.

4. Integrated Manufacturing To Mitigate CMC Risks, Simplify Commercial Supply 10/15/2025

   Leveraging cross-functional coordination between sites, harmonized tech transfers, one quality system, and synchronized team activities can streamline regulatory submissions and deliver high-quality commercial outcomes.

5. Driving Operator Safety And Process Efficiency 10/14/2025

   Discover how ergonomic design and workflow simplification can turn routine production tasks into strategic advantages, as well as practical ways to boost safety, efficiency, and innovation.

6. From First-In-Human To Proof-Of-Concept — Quicker, Smarter, Streamlined 10/14/2025

   Explore examples of smarter SAD/MAD trial designs including multi-part and hybrid protocols, regulatory foresight, recruitment considerations, and operational strategies that keep programs moving.

7. Evolving Gene Editing For Rare Disease Drug Development 10/9/2025

   Explore how scalable gene editing platforms are advancing therapies for ultra-orphan conditions, with insights into manufacturing models, regulatory strategies, and clinical approaches.

8. Compliance To Confidence: Annex 1 For Small-Batch, High-Value Production 10/3/2025

   Get strategies for meeting the updated GMP Annex 1 in small-batch aseptic filling. Learn about contamination control, quality management, and equipment design for high-value liquid and powder products.

9. Liquid Phase Peptide Synthesis: Regulatory, Analytical, And QC Perspectives 10/3/2025

   Discover how Liquid Phase Peptide Synthesis (LPPS) uses traditional reactors to create more efficient and sustainable peptide manufacturing. Learn about key analytical and quality control considerations.

10. Supply Resiliency For Bioprocessing Amid Global Volatility 10/2/2025

    Build bioprocessing resiliency with strategic supply chain management. Learn to meet quality, compliance, and time-to-market demands amid global volatility with effective sourcing.