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Join us for a comprehensive examination of Annex 1, emphasizing on Quality Risk Management, data integrity, contamination control, sterility, and integrity assurance.
Gain insights into sterile filtration, SU filtration solutions, integrity testing, Single-Use Systems and the collaborative responsibilities of end-users and suppliers in aseptic manufacturing for emerging therapeutic modalities.
We will also discuss the risks associated with single-use technologies with respect to robustness, integrity, sterility, and interactions with the product.
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