| dc.description.abstract | Background: Based on Government Regulation of the Republic of Indonesia
Number 51 of 2009, pharmaceutical work includes the manufacture and quality
control of pharmaceutical preparations, security, procurement, storage, and
distribution or dispensing of medicines, medicine management, prescription
medicine services, medicine information services, and the development of
medicines, medicinal ingredients, and traditional medicines. The production of
pharmaceutical preparations or the manufacture of a pharmaceutical preparation is
one of the means of carrying out pharmaceutical work in the pharmaceutical
industry, and pharmacists play an important role in this. Objective: This study aims
to determine the role and responsibilities of pharmacists at PT. Abbott Indonesia
and to understand the implementation of Good Manufacturing Practices (GMP) at
PT. Abbott Indonesia. Method: The method used was observation and direct
practice by students in PKPA activities carried out from January 6 to February 28,
2025, at PT. Abbott Indonesia. Student activities during PKPA included
qualifications in design, installation, operations, and performance, as well as
validation, which is a process to ensure that verified data or information meets the
standards at PT Abbott Indonesia. Conclusion: Pharmacists at PT. Abbott
Indonesia have roles and responsibilities as key personnel in production, quality
control, and quality assurance in guaranteeing the quality of the products produced.
In addition, PT. Abbott Indonesia has implemented CPOB aspects well, as
evidenced by its CPOB certificate.
Keywords: Pharmacist Professional Practice, pharmaceutical industry,
qualification, validation, Good Manufacturing Practices. | en_US |
