Building a Regulatory Roadmap for In Vivo Gene Engineering
Time: 2:30 pm
day: Pre-Conference Workshop Day
With the entire cell and gene space on the cusp of a massive shift into the in vivo space, the field is still lacking clarity around regulatory requirements and expectations due to the nascent and ever-evolving nature of this field.
Attend this workshop to:
• Understanding how the regulatory authorities are going to look at these novel types of in-vivo therapeutics
• What preclinical testing is going to be required?
• Exploring the clinical safety measures that need to be demonstrated to the regulatory authorities