Calidi presented its manufacturing process for CLD-401 at the 9th Annual Bioprocessing Summit in Barcelona. The company said it has received FDA feedback through a Type D meeting request process related to its manufacturing and analytical approaches for CLD-401. Antonio Santidrian and Eric Poma spoke about the manufacturing strategy and regulatory interactions during the event.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Calidi Biotherapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603120800PRIMZONEFULLFEED9670704) on March 12, 2026, and is solely responsible for the information contained therein.
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