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As demand continues to grow, pharmacists are increasingly seeing the real-world clinical and operational challenges associated with: inconsistent follow-up rapid titration escalation fragmented care coordination medication switching due to coverage changes and patients remaining on therapies without appropriate reassessment of tolerability or clinical response Expanding access matters

Certified impurity standards play a vital role in quantifying impurity levels, ensuring batch-to-batch consistency, and supporting analytical method validation

Furthermore, data on duration and dose of GLP-1 agonist use was not considered