Phase-Appropriate Plasmid DNA Manufacturing for Cell & Gene
Therapy

Download the Aldevron Article

region na1
portalId 1769030
formId 9d3608e8-4663-469a-a457-b159c2fbbd2b
target services-hubspot-form
redirectUrl https://www.aldevron.com/thank-you/whitepaper-empowering-future-cell-gene-therapy

Empowering the Future of Cell and Gene Therapy

Explore how Aldevron’s GMP-Source™ and Small-Scale cGMP services provide scalable, cost-effective, and regulatory-ready plasmid DNA manufacturing solutions tailored to early-stage clinical trials.

What You'll Learn

  • The difference between GMP-Source™ and Small-Scale cGMP
  • How phase-appropriate manufacturing accelerates timelines and reduces costs
  • Why Aldevron’s model supports seamless transition to full cGMP
  • Strategic insights for early-stage CGT developers navigating regulatory complexity

Why It Matters

Cell and gene therapy developers face unique challenges in early-stage manufacturing. Our approach helps you:

  • Avoid costly delays and inefficiencies
  • Maintain regulatory confidence
  • Scale with precision and flexibility
  • Leverage 20+ years of manufacturing expertise

Download the Aldevron article now to unlock the future of CGT