T/ZCHSP 002-2023 Active

Main technical content: This standard mainly stipulates the specific requirements of the following technical parameters, as detailed below: (1) Basic requirements ① Personnel requirements: Refer to the “Guidelines for Pharmaceutical Reconciliation Services in Medical Institutions” issued by the National Health Commission (No. [2021]520) ② Hardware and software requirements: Refer to foreign pharmaceutical reconciliation experiences: “An Introduction to Pharmaceutical Reconciliation Work by Clinical Pharmacists in Foreign Countries” [J]. Drug Evaluation, 2012, 9(32): 6–9 ③ Timing of reconciliation: Refer to Article 22 of the “Basic Standards for Medical Record Writing” issued by the National Health Commission (No. [2010]11) regarding the writing deadlines for first medical records and surgical records, as well as the actual needs of clinicians and patients for preoperative pharmaceutical reconciliation ④ Training based on the actual needs of pharmacists conducting pharmaceutical reconciliation (2) Quality control ① Regular inspections of pharmaceutical reconciliation work by competent authorities: Refer to the “Guidelines for Pharmaceutical Reconciliation Services in Medical Institutions” issued by the National Health Commission (No. [2021]520) ② Continuous improvement of pharmaceutical reconciliation quality: Refer to the “Guidelines for Pharmaceutical Services in Medical Institutions” (2019 Edition) and the “Guidelines for Pharmaceutical Reconciliation Services in Medical Institutions” issued by the National Health Commission (No. [2021]520)