T/ZCHSP 006-2024 Active

Main technical content: Terms and Definitions Chapter: Provides five terms related to pregnancy medication, medication consultation, medication consultation outpatient clinics, follow-up, and pregnancy follow-up. The sources of these terms are referenced in the *Internet Pharmaceutical Services Work Standards (Trial)*. Basic Requirements Chapter: Specifies the basic requirements for follow-up work for patients in pregnancy medication consultation outpatient clinics, including personnel requirements and equipment/software requirements. The personnel requirements are based on the qualification requirements for medication consultants outlined in the *Zhejiang Province Supervision and Management Measures for the Use of Drugs and Medical Devices in Medical Institutions* (Zhejiang Provincial People's Government Decree No. 238 of September 19, 2007) and the *Notice on Issuing Five Norms for Pharmaceutical Outpatient Services in Medical Institutions* (Guo Wei Ban Yi [2021] No. 520). Follow-up Objects and Models Chapter: Defines the follow-up objects and models, including face-to-face follow-up, phone follow-up, SMS/WeChat follow-up, and IT-assisted follow-up. Based on practical experience, it provides diagrams and charts for follow-up operational processes and outcomes. Follow-up Process Chapter: Specifies information collection and evaluation, follow-up plan establishment, follow-up questionnaire design, follow-up time setting, follow-up task execution, and pregnancy outcome tracking. The follow-up time setting refers to the main prenatal checkpoint dates in obstetrics and extends them by one to several weeks to facilitate timely recording of examination results. Based on practical experience, it provides appendices including follow-up operational processes, follow-up record forms, and types of birth defects. Quality Control Chapter: Defines requirements for quality management and continuous improvement to ensure the implementation of follow-up work for patie