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Genetic therapies utilizing adeno-associated viral (AAV) vectors have evolved in recent years from proof of concept to successful treatment options for patients with previously difficult to treat diseases. However, to be successful for multiple and larger patient populations, these groundbreaking therapies must overcome the critical challenge of manufacturing at a scale that meets the growing global need.
Access this valuable resource to discover how developers working on larger indications or patient populations can efficiently manufacture at necessary scales while still providing high-quality, safe, and effective drug products. You’ll learn about:
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