Formulation Development White Papers & Articles

  1. Cell Culture Media Demystified For Performance, Quality, And Innovation 11/13/2025

    Cell culture media isn’t one-size-fits-all. Learn how media composition, customization, and analytics can dramatically improve cell growth, productivity, and product quality for complex processes.

  2. Calcium Carbonate Vs Titanium Dioxide: Why Particle Engineering Matter 11/10/2025

    Discover how particle-engineered calcium carbonate offers a viable alternative to titanium dioxide in tablet coatings, achieving good opacity, process efficiency, and comparable tablet properties.

  3. Isolate Bright GFP-Expressing HEK293 Cells For Cell Line Development Workflow 11/7/2025

    Explore a high-efficiency workflow for isolating and expanding GFP-expressing HEK293 cells that enables stable, bright clones ideal for imaging and tracking to simplify clonal development.

  4. Generate CHO-K1 GFP-Expressing Cells For Cell Line Development Workflow 11/7/2025

    Discover a high-efficiency workflow for generating GFP-expressing CHO-K1 clones using automated single-cell dispensing to achieve 93% isolation success and stable expression in under five weeks.

  5. API In Capsule Vs. The Lost Art Of Formulation Development 11/5/2025

    API-in-capsule offers a fast path for early clinical data, but it can't eliminate the need for full formulation development. Weighing the potential for higher total development time and cost is critical.

  6. Tools For Efficient And Reliable Gene Therapy Manufacturing 11/5/2025

    Discover scalable strategies for overcoming AAV purification challenges, from low yield and impurity removal to serotype variability, as well as how advanced tools can streamline manufacturing.

  7. Enabling The Future Of Intensified Biomanufacturing 11/5/2025

    Process intensification demands smarter orchestration, real-time analytics, and scalable automation. Discover how digital infrastructure enables synchronized, compliant, and predictive biomanufacturing.

  8. Advancing Multiomics Through Intelligent Automation 10/27/2025

    Modern automation tackles hidden pipetting errors and boosts reproducibility. Discover how your lab can scale confidently, reduce rework, and accelerate multiomic workflows with built-in traceability.

  9. Tackling Poor Bioavailability With Early Formulation Strategies 10/24/2025

    Poor oral bioavailability causes high clinical trial failure rates. Learn how to identify and apply the correct enabling formulation strategy early in development to de-risk your program and accelerate timelines.

  10. Why Manual QbD Leads To Delays, Errors, And Ongoing Frustrations 10/24/2025

    Manual QbD methods slow timelines and increase risk. Learn how intelligent, digital frameworks are helping CMC teams improve quality, accelerate submissions, and meet rising regulatory expectations.