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November 2-4, 2020
Hilton San Francisco Union Square,
San Francisco, CA

Precise, efficient & safer genome editing – changing the face of genetic disorders and rare disease

Revolutionizing novel tech with CRISPR, Zinc Finger, Talens, Base Editing, RNA Editing, Mega nucleases and more...

Applications of Gene Editing Has Been Rescheduled to November 2-4, 2020

Our team is pleased to announce that Applications of Gene Editing is now rescheduled for November 2-4, 2020 at the Hiton Union Square, in San Francisco, CA.

We truly appreciate the outpouring of positive feedback received from our customers and colleagues within the Next Generation CAR & T Cell Therapies community. Rescheduling an event comes with challenges, but the safety and experience of everyone involved is our top priority and we’re committed to following the guidance of the local authorities.

Here's what the rescheduled event means for you:

Attendees: Your registration will automatically carry over to the new dates and you do not need to re-register. Should you have any questions, please contact our customer service team at

Speakers: Over the next few days our production team will contact you to reconfirm your participation as a speaker during our rescheduled dates.

Sponsors and Exhibitors: All contracts will be automatically applied to the new dates, leaving all Exhibit spaces and Sponsorship the same as originally contracted.

We wish to thank those who participate in, and support, Applications of Gene Editing and we greatly appreciate your patience and understanding.

Technological Advances & Applications in Genome Editing

Enabling more Precise and Efficacious Genome Editing & Quantifying its Outcomes
  • Get to grips with the repurposing of CRISPR-Cas 9 and all its variants  
  • Exchange ideas on tools for on and off target effects when using different enzymes & variants
  • Understanding on-target cutting – analyzing events at the intended site
Delivery, Administration & Editing Applications for Genetic Disease
  • Become an expert on non-viral delivery methods including nano injection, nanoparticles and more…
  • Simplify in vivo approaches to eye disease & DMD treatment
  • Discuss CRISPR and potential treatment strategies in blood and liver disorders
Novel Gene Editing Applications in CART
  • Understand next generations technologies in adoptive T cell immunotherapy
  • Prepare for allo CAR & T Cell Therapies – iPSc, Gene editing & highly characterized products
  • Build controls for product quality & specifications around gene editing


Benchmark against your peers

Therapeutic developers face real challenges with genetic diseases and immune-oncology; what to edit, how to edit and how to deliver your product are all key – make sure you aren’t the one being left behind.

The process is the product

How you make your product can sink or swim your business. What’s the point in building a product that costs more to make than it does to sell, or is only stable for 8hrs when it takes 10hrs to get it from the manufacturing facility to the patient?

Be a Leader

Companies continue to partner and work together in developing novel approaches to rare diseases – are you one of the ones driving the industry forward?


Whether you're increasing your company profile, launching a new product or focusing on new business development opportunities, collaborate with us to identify custom solutions to help you reach your goals.  

Contact Kristen Schott: | +1 857 504 6685


A week-long series of free webinars with live Q&A continues to connect cell and gene therapy leaders throughout the year from the comfort of your desk, hear the latest updates from leading industry speakers and gain an insight into some of the most innovative topics and research. 

Don't miss out this year's DIGITAL WEEK: 20-23 APRIL 2020

Registration now open

Silver Sponsors