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Manuscript source: Unsolicited manuscript Peer-review started: October 7, 2019 First decision: November 27, 2019 Article in press: January 19, 2020 Specialty type: Gastroenterology and hepatology Country of origin: Croatia Peer-review report classification Grade A (Excellent): 0 Grade B (Very good): 0 Grade C (Good): C Grade D (Fair): 0 Grade E (Poor): 0 P-Reviewer: Dragoteanu MN S-Editor: Ma YJ L-Editor: A E-Editor: Wu YXJ Contributor Information Slaven Gojkovic, Departments of Pharmacology and Pathology, Medical Faculty University of Zagreb, Zagreb 10000, Croatia

doi: 10.1016/j.eprac.2020.10.014

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We follow the highest safety and quality standards in IV compounding

Pharm Res 1999 (PMID 10496658) (PubMed) [7] FDA: Medications Containing Semaglutide Marketed for Type 2 Diabetes or Weight Loss (FDA) [8] FDA Alerts Health Care Providers, Compounders, and Patients of Dosing Errors Associated With Compounded Injectable Semaglutide Products (FDA) [9] FDA: Certain Bulk Drug Substances for Use in Compounding May Present Significant Safety Risks (503A Category 2), including the table of substances previously in Category 2 whose nominations were withdrawn by the nominators, which now lists BPC-157 (FDA) [10] FDA Briefing Document, Pharmacy Compounding Advisory Committee meeting July 23-24, 2026: FDA evaluation of BPC-157-related bulk drug substances