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08 19 21 -- Top Priorities And Challenges For New CDER Director Patrizia Cavazzoni, M D

08 19 21 -- Top Priorities And Challenges For New CDER Director Patrizia Cavazzoni, M D
pharmaceuticalonline.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmaceuticalonline.com Daily Mail and Mail on Sunday newspapers.

06 24 21 -- FDA s Codifies New Chemical Entity Designations Approach

06 24 21 -- FDA s Codifies New Chemical Entity Designations Approach
pharmaceuticalonline.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from pharmaceuticalonline.com Daily Mail and Mail on Sunday newspapers.

01 21 21 -- Using Production And Postmarket Data To Validate FMEA Assumptions

01.21.21 Using Production And Postmarket Data To Validate FMEA Assumptions   Acepodia s Dr. Sony Hsiao, CEO, and Dr. Mark Gilbert, SVP of R&D, join Business of Biotech for a discussion on the company s approach to dramatically reducing the cost of cell therapy development, manufacturing, and administration via its oNK, CAR, and ACC candidates. Listen now and subscribe so you never miss an episode. Featured Editorial By Mark Durivage, Quality Systems Compliance LLC One common issue with regulatory agencies and certification bodies regarding failure mode and effects analysis (FMEA) is that organizations are not utilizing production and post-market surveillance data to validate the probability of occurrence and probability of detection assumptions, which leads to inspectional observations and audit findings.

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