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According to FDAs recommendations, a two-step deduplication process was used to ensure the unique report: 1) selecting the higher primaryid when the caseid and fda_dt were the same, 2) selecting the latest fda_dt when caseid were the same, where primaryid was an unique number for identifying a AE report, caseid was an unique number for identifying a case, and fda_dt was the date when FDA received a case ( Figure 1 )

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We start with comprehensive testing and a goals review, decide whether this triple-peptide protocol fits your biology, and monitor your response over a defined cycle

We ensure this by putting each batch through rigorous purification processes and quality tests