2022 - AAV Manufacturing — Overcoming the Challenges of Plasmid DNA
Date2022-11-30
Deadline2022-11-30
VenueWebinar, USA - United States
KeywordsDrug Development; Plasmid DNA; PDNA
Topics/Call fo Papers
AAV manufacturing and other types of advanced therapy production are experiencing challenges associated with their plasmid DNA supply. This includes slow or delayed production and poor DNA quality (owing to unstable or difficult sequences), impacting their ability to meet drug development timelines and regulatory demands.
In this webinar, the featured speakers will address the challenges of plasmid DNA in AAV manufacturing and present data and supportive case studies which introduce an alternative to plasmid DNA — an enzymatic, antibiotic-free DNA vector called doggybone DNA (dbDNA™).
Register to learn how doggybone DNA can eliminate many issues around complex or unstable sequences in AAV production, alongside improved speed to manufacture, safety and scalability.
In this webinar, the featured speakers will address the challenges of plasmid DNA in AAV manufacturing and present data and supportive case studies which introduce an alternative to plasmid DNA — an enzymatic, antibiotic-free DNA vector called doggybone DNA (dbDNA™).
Register to learn how doggybone DNA can eliminate many issues around complex or unstable sequences in AAV production, alongside improved speed to manufacture, safety and scalability.
Other CFPs
- Risk Assessment: Traditional and Novel Approaches to Assess and Manage Risks
- Constructing a Pharma Development & Manufacturing Project Plan: Steps to Evaluate Risk & Find Efficiencies
- Scaling DCTs to Drive the Transformation of Clinical Development
- FROM-16: Measuring the Hidden Burden of Family Impact of Disease
- Creating a Global CMC Dossier to Achieve Operational Readiness
Last modified: 2022-11-02 02:11:20