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Dokumento informacija
4.5 Requirements for reporting Serious Adverse Events (SAEs) and Serious Adverse Drug Reactions (ADRs) from Clinical Trials (CTs) conducted in the Republic of Lithuania to the State
Aprašymas Requirements for reporting Serious Adverse Events (SAEs) and Serious Adverse Drug Reactions (ADRs) from Clinical Trials (CTs) conducted in the Republic of Lithuania to the State Medicines Control Agency of Lithuania (SMCA)
