Relevance. Extemporaneous manufacturing of preparations is an important component of modern patient-oriented medicine. This article provides an analysis of regulatory documents regulating the manufacture of drugs in a pharmacy, identifies problems and weaknesses in rationing production, and proposes constructive ways to solve the problems presented.Methodology. When conducting the study, methods of content analysis, comparative and logical analysis, and observation were used.Results. This article provides a critical analysis of the legal framework regulating the extemporaneous production of drugs. Weaknesses in the regulation of pharmaceutical production of dosage forms have been identified. In particular, the following problems are presented: checking the doses of active pharmaceutical substances and assessing the compatibility of prescription ingredients; issues related to the expiration dates of extemporaneously manufactured medicinal products; and problems with regulating conditions for the manufacture of drugs in pharmacies. Difficulties in equipping pharmacies with small-scale mechanization and aspects of the provision of modern active pharmaceutical ingredients and excipients are reflected, and the potential of physicians in prescribing extemporaneous prescriptions is noted.Conclusion. The proposed solutions to the identified problems will allow extemporaneous production to a new, more advanced level and expand the capabilities of personalized medicine.