Newsletter | March 8, 2023

03.08.23 -- Understanding The Gene Therapy Manufacturing Process
 
Navigating Analytical Requirements For GMP Viral Vectors
 

The keys to success are establishing appropriate strategies and fundamental testing, expecting additional regulatory requests, being prepared for assay variability, recognizing the limits of current understanding, and ensuring that comparability studies will be possible by retaining material from preclinical batch runs and stability studies.
AAV Vector Manufacturing
 

Due to its therapeutic impact on a wide range of diseases and disorders, adeno-associated virus (AAV) gene therapy is one of the most promising advances in modern medicine. Understand how AAV vectors and plasmids are produced.
What To Consider When Looking To Partner With A CDMO
 

It’s not just about scheduling, capacity, and terms. In this Q&A, an industry expert shares his views on overlooked considerations when partnering with a CDMO and the challenges of building a new facility during a pandemic.
Understanding The Gene Therapy Manufacturing Process
 

Gene therapy is the process of replacing damaged or unhealthy genetic material with new material for treating various diseases and conditions. Curious to learn more about the process of gene therapy manufacturing? Explore the steps that go into manufacturing a gene therapy treatment.
Solutions
The Andelyn Difference

For this innovative biotech, the patient always comes first. With over 15 years of experience in gene therapy research, Andelyn Biosciences brings pioneering solutions that turn hope into reality.
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Registration is open! See for yourself why Outsourced Pharma Capacity Update has become a wildly popular resource to identify options for your development and manufacturing needs. Join us March 7th – 9th as leading CDMOs in Biologics, Cell & Gene, and Small Molecule share their capabilities and available capacities. Register here for the virtual event!

 

For added convenience, Outsourced Pharma Capacity Update is grouped by molecule type. You can register for the session(s) highlighting the CDMOs equipped to meet your company's development and manufacturing needs.