研制mRNA-bnt162B2疫苗的组织模式:都灵Mauriziano医院药房临床盖伦学实验室的经验

Eleonora Chiaramonte, Kristela Bushkolaj, Paolo Aluffi, Rosanna Borello, Giusi Galota, Annalisa Luchin, Emma Miotto, Antonietta Smaldone, Domenico Tripodi, Mario Michelotti, Marco Bellero, Alessandra Bianco, Giovanna Fazzina, Maddalena Marcato, Simona Masucci, Danilo Pennetta, Maria Carmen Azzolina, Annalisa Gasco
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摘要

在都灵Mauriziano医院药房临床Galenics实验室集中制备mRNA-bnt162B2疫苗是一种组织模式,旨在保证所给药物的质量、接种者和接种人员的安全以及所进行的所有操作的可追溯性。根据《官方药典》的良好生产规范(GMP),将即用型注射器的制备单独包装和贴标签,委托给医院药剂师负责的生物医学实验室技术员(BLT)。根据GMP,该模型是通过专门的场所、专门的工作人员培训和有关疫苗处理的书面程序开发的。整个生产过程由以下人员保证:一名医院药剂师和两名可互换的blt,一名制备人员和一名助理。它们对于保持无菌技术和所有操作的交叉检查是必要的。制作标签,显示定性定量组成,批号和有效期,制剂的有效性,药剂师的签名。每个注射器上的标签以及日常工作计划,确保了每个阶段过程的可追溯性。所提出的有效模型一直被证明能够适应疫苗接种运动所特有的变化。从2020年12月27日至2022年3月31日,共制备了48.017剂。将疫苗制备集中在医院药房临床盖伦学实验室也减少了处理错误,以及未使用残留物的浪费,这一比例仅为0.08%。
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Development of an organisational model for the preparation of the mRNA-bnt162B2 vaccine: the experience of the Clinical Galenics Laboratory of the Hospital Pharmacy of the Mauriziano Hospital, Turin
The centralised preparation of the mRNA-bnt162B2 vaccine at the Clinical Galenics Laboratory of the Hospital Pharmacy of the Mauriziano Hospital in Turin is an organisational model designed to guarantee the quality of the drug to be administered, the safety of both the vaccinee and the vaccinating personnel, and the traceability of all operations performed. The preparation in ready-for-use syringes individually packaged and labelled, according to the Good Manufacturing Practice (GMP) of the Official Pharmacopoeia, was entrusted to the Biomedical Laboratory Technician (BLT) under the responsibility of the Hospital Pharmacist.In compliance with the GMP, the model was developed through dedicated premises, specific staff training and written procedures concerning the handling of vaccines. The entire production process was guaranteed by: a Hospital Pharmacist and two interchangeable BLTs, one preparer and one assistant. They were necessary to maintain the aseptic technique and the cross-checking of all operations. Labels were prepared showing qualitative-quantitative composition, batch and expiry date, validity of the preparation, pharmacist’s signature. The label applied to each syringe, together with the daily work plan, ensured traceability of the process at every stage.The efficient model proposed has always proved adaptable to the changes that characterised the vaccination campaign. From 27/12/2020 to 31/03/2022 a total of 48.017 doses were prepared. The centralisation of the vaccine preparation in the Clinical Galenics Laboratory of the Hospital Pharmacy also reduced handling errors, as well as the waste from unused residues, which proved to be only 0.08%.
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