• understanding the concept of “quality” in medicine and pharmacy; description the concept of quality assurance for drugs; naming of the main indicators of quality of medical and pharmaceutical technologies; specification of factors that affect the quality of drugs; description of principles of rational use of drugs; understanding of principles of quality assurance in medical technologies; to formulation of principles of quality evaluation in medical technologies.
• determination of principles for finding new drugs and scientific approaches to their creation; describing the system of examination of new drugs; specification of sources of information about drugs; description of principles of launching and use of new drugs on the pharmaceutical market; formulation of tasks of scientific research in the field of creation of new drugs; development of scheme of pharmacological experiment counting ethical, deontological aspects, main indicators of information security; searching and carry out analytical work with information regarding the creation and use of drugs;

Disciplines, required to be studied before the course:
Pharmaceutical Biochemistry and Regulatory support for the registration of new drugs.
Disciplines, required to be studied during the course:
Clinical and pharmaceutical basics of drug production (principles of searching new drugs, research into new drugs, implementation of new drugs into the therapeutic treatment).
Evaluation of quality of medical and pharmaceutical technologies (quality of drugs, quality of treatment).

Clinical-pharmaceutical and clinical-pharmacological principles of the choice of drugs for rational pharmacotherapy. Ethical-deontological and bioethical problems of the use of drugs. The system of protection of the rights of the patient, the doctor, the average medical worker, the clinical pharmacist and of the pharmacist. Informed consent of the patient for medical and pharmaceutical intervention. Modern principles of clinical trials. Evaluation of bioavailability and bioequivalence of drugs their role in the rational use of drugs. The role of evidence-based medicine and pharmacy in the rational use of drugs. Rational use of drugs in the framework of the implementation of the form system. Pharmacoepidemiology and pharmacoeconomics as a basis for rational use of drugs. Principles of rational use of medicines for patients of different age categories or with bad habits. Clinical and pharmaceutical aspects of treatment of pain syndrome of different etiology.

1. Аткинсон А.Дж. Принципы клинической фармакологии. Перевод с
англ. / под ред. Сухих Г.Т. М.: Изд. «Практическая медицина», 2013. - 530 с.
2. Зборовский А.Б., Тюренков И.Н., Белоусов Ю.Б. Неблагоприятные
побочные эфффекты лекарственных средств. – М.: ООО «Медицинское
информационное агентство», 2008. – 656 с.
3. Клиническая фармакология и фармакотерапия в реальной врачебной
практике. Мастер-класс: учебник / В.И. Петров. – М.: ГЭОТАР-Медиа,
2011. - 880 с.
4. Клиническая фармакология: учебник / под ред. О.Я. Бабака, А.Н.
Беловола, И.С. Чекмана. – Киев : ВСИ «Медицина», 2012. – 728 с.
5. Клінічна фармакологія: підруч. для студ. внз: в 2 т. / С.В. Нальотов, І.А.
Зупанець, Т.Д. Бахтєєва та ін.; за ред. І.А. Зупанця, С.В. Нальотова, О.П.
Вікторова. – Х.: Вид-во НФаУ: Золоті сторінки, 2007. – Т. 1. – 348 с.

• Continuous assessment: written-oral exam and defense of reports of practical works - 30 points;
• Final control - 70 points (exam): written-oral form.

• understanding the concept of “quality” in medicine and pharmacy; description the concept of quality assurance for drugs; naming of the main indicators of quality of medical and pharmaceutical technologies; specification of factors that affect the quality of drugs; description of principles of rational use of drugs; understanding of principles of quality assurance in medical technologies; to formulation of principles of quality evaluation in medical technologies.
• determination of principles for finding new drugs and scientific approaches to their creation; describing the system of examination of new drugs; specification of sources of information about drugs; description of principles of launching and use of new drugs on the pharmaceutical market; formulation of tasks of scientific research in the field of creation of new drugs; development of scheme of pharmacological experiment counting ethical, deontological aspects, main indicators of information security; searching and carry out analytical work with information regarding the creation and use of drugs;

Disciplines, required to be studied before the course:
Pharmaceutical Biochemistry and Regulatory support for the registration of new drugs.
Disciplines, required to be studied during the course:
Clinical and pharmaceutical basics of drug production (principles of searching new drugs, research into new drugs, implementation of new drugs into the therapeutic treatment).
Evaluation of quality of medical and pharmaceutical technologies (quality of drugs, quality of treatment).

Clinical-pharmaceutical and clinical-pharmacological principles of the choice of drugs for rational pharmacotherapy. Ethical-deontological and bioethical problems of the use of drugs. The system of protection of the rights of the patient, the doctor, the average medical worker, the clinical pharmacist and of the pharmacist. Informed consent of the patient for medical and pharmaceutical intervention. Modern principles of clinical trials. Evaluation of bioavailability and bioequivalence of drugs their role in the rational use of drugs. The role of evidence-based medicine and pharmacy in the rational use of drugs. Rational use of drugs in the framework of the implementation of the form system. Pharmacoepidemiology and pharmacoeconomics as a basis for rational use of drugs. Principles of rational use of medicines for patients of different age categories or with bad habits. Clinical and pharmaceutical aspects of treatment of pain syndrome of different etiology.

1. Аткинсон А.Дж. Принципы клинической фармакологии. Перевод с
англ. / под ред. Сухих Г.Т. М.: Изд. «Практическая медицина», 2013. - 530 с.
2. Зборовский А.Б., Тюренков И.Н., Белоусов Ю.Б. Неблагоприятные
побочные эфффекты лекарственных средств. – М.: ООО «Медицинское
информационное агентство», 2008. – 656 с.
3. Клиническая фармакология и фармакотерапия в реальной врачебной
практике. Мастер-класс: учебник / В.И. Петров. – М.: ГЭОТАР-Медиа,
2011. - 880 с.
4. Клиническая фармакология: учебник / под ред. О.Я. Бабака, А.Н.
Беловола, И.С. Чекмана. – Киев : ВСИ «Медицина», 2012. – 728 с.
5. Клінічна фармакологія: підруч. для студ. внз: в 2 т. / С.В. Нальотов, І.А.
Зупанець, Т.Д. Бахтєєва та ін.; за ред. І.А. Зупанця, С.В. Нальотова, О.П.
Вікторова. – Х.: Вид-во НФаУ: Золоті сторінки, 2007. – Т. 1. – 348 с.

• Continuous assessment: written-oral exam and defense of reports of practical works - 30 points;
• Final control - 70 points (exam): written-oral form.