Downstream Challenges with Complex Injectables
WEBINAR
As per the US Food and Drug Administration (FDA), complex parenteral products are those formulations which contain either complex ingredients or API, complex formulation, i.e. delivery carrier, complex route of administration, complex dosage form, or complex drug device combination. The manufacturing of the complex injectable products is different and a great level of observation of quality and care is required during their manufacturing, packaging, distribution, and storage. Complex injectables have gained increasing attention due to their widespread use in life-threatening and chronic diseases treatments. The category includes diabetes, oncology, and hormonal therapy.
In this webinar, you will learn:
- Why downstream processing (specifically sterile filtration) is critical and complicated
- About the sterile filtration of liposomes, nanoparticles, and viscous formulations
- About filter validation aspects and where our approach is different
Speaker

Partha Banerjee
Merck
Technical Application Expert, Downstream India
Partha Banerjee is a Technical Application Expert at Merck with over 17 years of experience in downstream bioprocessing and biopharmaceutical process development. He specializes in sterile filtration, filter optimization, troubleshooting, and regulatory-aligned validation strategies. Known for translating scientific concepts into practical solutions, he supports biopharma manufacturers in achieving robust and compliant processes. Partha holds a Master’s degree in Pharmaceutical Chemistry and has expertise in IPR and patent management.
Pharma and biopharma manufacturing
- Downstream Processing
Czas trwania:1h
Język:English
Sesja 1:pokazane March 29, 2022