Development of documents on GMP standards for the production of medicines . Methodical recommendations” is a unique publication created by the team of authors, which will become an indispensable assistant for specialists in the field of pharmaceuticals, as well as for students and teachers of specialized educational institutions .. In today's market, where the requirements for the quality and safety of medicines are becoming more stringent, knowledge of GMP (Good Manufacturing Practice) standards becomes necessary for successful work in this area. This publication discusses in detail the key aspects of the development of documentation that meets international standards GMP. The authors offer readers not only a theoretical basis, but also practical recommendations that will help in creating and implementing an effective quality management system in pharmaceutical enterprises. Each chapter of the book is riddled with relevant information that will help to understand the intricacies and nuances associated with the development of the necessary documents, such as instructions, regulations and protocols. The book will be of particular interest to pharmaceutical professionals, including quality managers, regulatory specialists, as well as anyone involved in the production and quality control of medicines. Students and graduate students studying pharmaceutical sciences will find useful materials in this publication that will help them better understand the practical application of theoretical knowledge. It will also be useful to teachers who are looking for relevant and practical examples for their courses. The topics raised in the book cover a wide range of issues related to quality assurance at all stages of drug production. The authors emphasize the importance of documenting processes, which is a key element in compliance with GMP standards. Readers will be able to learn about how to properly develop and draw up documents, what requirements are imposed on their content and structure, as well as how to conduct internal audits and ensure the continuous improvement of processes. The style of the authors is distinguished by clarity and accessibility of presentation, which makes the material understandable even for those who are just starting their way in the pharmaceutical industry. The book is filled with examples from practice, which allows readers to see how theoretical knowledge is applied in real conditions. This makes the publication not only a tutorial, but also a practical guide that can be used in everyday work. If you are looking for literature that will help you understand GMP standards and teach you how to develop high-quality documentation for pharmaceutical production, then “Development of documents according to GMP standards for the production of medicines . Guidance” will be your reliable companion This publication will not only expand your knowledge, but also help you become a more competitive specialist in the rapidly changing world of pharmaceuticals. Do not miss this important book, which will become your guide in the world of quality standards and safety of medicines Read, learn and apply the knowledge gained in practice - and you will definitely achieve success in your professional activities!