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S. Raymond Golish, MD, PhD, MBA, FAAOS; Ryan Pezold, MA; David S. Jevsevar, MD, MBA, FAAOS
The FDA has formally ended the “enforcement discretion” of its comprehensive policy framework on biologics and regenerative medicine products.
Terry Stanton
In July, the Board of Directors approved a Clinical Practice Guideline (CPG) and an accompanying set of Appropriate Use Criteria (AUC) on Pharmacologic, Physical, and Cognitive Pain Alleviation for Musculoskeletal Extremity/Pelvis Surgery.
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