Frost & Sullivan
Frost & Sullivan

Gene Therapy Process Development 2.0 – What’s Next?

Gene therapy continues to experience explosive growth driven by the development of better assays, more-frequent outsourcing to contract development and manufacturing organizations (CDMOs), greater capital investment, and the rise of plug-and-play platform technologies. Still, challenges loom: viral vectors can cause unwanted immune responses, standardized analytics and assays lag, regulatory guidance is still forming, and manufacturing remains difficult and expensive, resulting in unaffordable prices. How will challenges and potential breakthroughs affect the future of gene therapy process development?

Download this complimentary Article to discover:

  • The Regulatory Environment of Gene Therapy Process Development
  • Opportunities for Cell and Gene Therapy
  • New Trends and the Future of Gene Therapy
  • Industry Leaders’ Perspective on Gene Therapy

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