| Issue | 
	Section | 
        Title | 
	File | 
											
				| Vol 50, No 9 (2016) | 
		Article | 
		Selection of Standardization Parameters and Development of Quality Control Methods for Isoleucyl-Tryptophan Dipeptide Coordination Complex with Iron(II) (Timofer) | 
		
					 | 
		
												
				| Vol 50, No 10 (2017) | 
		Drugs | 
		Interchangeability Criteria for Levofloxacin-Based Medicinal Products in the Russian Federation | 
		
					 | 
		
												
				| Vol 50, No 12 (2017) | 
		Drugs | 
		Planning Bioequivalence Studies of Drugs with Narrow Therapeutic Indices | 
		
					 | 
		
												
				| Vol 51, No 5 (2017) | 
		Drugs | 
		Influence of Human Biorhythms on the Blood Glucose Level and the Efficacy of Hypoglycemic Drugs (Review) | 
		
					 | 
		
												
				| Vol 51, No 6 (2017) | 
		Article | 
		Toxic and Immunomodulatory Properties of an Iron(II) Coordination Complex of Isoleucyltryptophan Dipeptide | 
		
					 | 
		
												
				| Vol 51, No 8 (2017) | 
		Article | 
		Optimization of Drug Administration Dosage Regimen Considering Chronorhythms and Desynchronosis of Gastrointestinal-Tract Organs | 
		
					 | 
		
												
				| Vol 51, No 8 (2017) | 
		Article | 
		Interchangeability Problems of Drugs with Narrow Therapeutic Indices | 
		
					 | 
		
												
				| Vol 51, No 11 (2018) | 
		Article | 
		Validation of a Quantitative Determination Method for Ormustine in a Lyophilized Dosage Form | 
		
					 | 
		
												
				| Vol 52, No 2 (2018) | 
		Article | 
		Development of a Sample-Preparation Procedure for Quantitative Determination of Lead in Sugars by Inductively Coupled-Plasma—Atomic-Emission Spectrometry (ICP-AES) | 
		
					 | 
		
												
				| Vol 52, No 4 (2018) | 
		Medicinal Plants | 
		Plant Juices and Related Medicinal Preparations: Issues of Standardization and Quality Control | 
		
					 | 
		
												
				| Vol 52, No 7 (2018) | 
		Article | 
		Synthesis and some Pharmacological Properties of an Immunoactive Lysine-Containing Tetrapeptide | 
		
					 | 
		
												
				| Vol 52, No 8 (2018) | 
		Structure of Chemical Compounds, Methods of Analysis and Process Control | 
		Standardization of Drug Substances According to the Purity Section | 
		
					 | 
		
												
				| Vol 52, No 10 (2019) | 
		Article | 
		Validation of Methods and Procedures in Pharmacopoeial Monographs in the Framework of a Drug Standardization Program | 
		
					 | 
		
												
				| Vol 52, No 11 (2019) | 
		Structure of Chemical Compounds, Methods of Analysis and Process Control | 
		Pharmacopoeial Quality Requirements for Medicinal Products | 
		
					 |