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1. Utilizing PAT to Monitor and Control Bulk Biotech Processes

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   Document | 27 Mar 2024 | Contributor(s):: Rick E. Cooley

   1.What is and isn’t PAT? 2.Implementing PAT in Manufacturing: What does it take? 3.Characteristics of bulk, biotech API processes 4.Why PAT? 5.Review of PAT technologies utilized 6.PAT application examples

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   Diyar Hassan

   Effective leader with 11+ years experienced Head of Pharmaceutical Quality Control laboratory and qualified person in pharmaceutical industry laboratory.I have a master’s degree in...

   https://cmkc.usp.org/members/1291

3. Recent advances in integrated process analytical techniques, modeling, and control strategies to enable continuous biomanufacturing of monoclonal antibodies

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   Peer-reviewed journal | 09 Jun 2023 | Contributor(s):: Chopda, Viki, Gyorgypal, Aron Yang, Ou Singh, Ravendra Ramachandran, Rohit Zhang, Haoran Tsilomelekis, George Chundawat, Shishir PS, Ierapetritou, Marianthi G

   Continuous bioprocessing is significantly changing the biological drugs (or biologics) manufacturing landscape by potentially improving product quality, process stability, and overall profitability, as was similarly seen during the adoption of advanced manufacturing processes for small molecule...