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Comparison of FDA (2018) and EAEU Regulatory Requirements for Bioanalytical Method Validation
Uvarova N., Eremenko N., Ramenskaya G., Goryachev D., Smirnov V.
HPLC-MS Method for Simultaneous Quantitative Determination of an Innovative Russian Gestagen and its Metabolites in Rat and Rabbit Blood Sera
Stepanova E., Makarenkova L., Chistyakov V., Rybakov Y., Gukasov V., Fedotcheva T., Parshin V., Votyakov V., Shimanovskii N.
Development and Validation of a Liquid Chromatography Method for the Analysis of Rivaroxaban and Determination of Its Production Related Impurities
Arous B., Al-Mardini M., Karabet F., Daghestani M., Al-Lahham F., Al-Askar A.
Validation of a Quantitative Determination Method for Ormustine in a Lyophilized Dosage Form
Bunyatyan N., Nikolaeva L., Olefir Y., Sanarova E., Oborotova N., Prokof’ev A., Ignat’eva E., Yartseva I., Gulyakin I.
Validation of Qualitative Microbiological Methods of Pharmaceutical Analysis
Gunar O., Builova I.
A Novel UV-Spectrophotometric Method for Simultaneous Estimation of Amlodipine and Captopril
Murtaza G., Akhtar Y., Mahmood T., Abid S., Makreski P.
Standardization of Thrombaptanib Drug Substance for Residual Organic Solvents
Petukhov A., Petrykina E., Tereshkina O., Ramenskaya G., Antipova O., Turashev A., Zav’yalova E., Golovin A., Pavlova G., Kopylov A.
Analytical Control of Darunavir Tablet Dosage Forms. Part I.
Goizman M., Korlyukov A., Suponitskii K., Shimanovskii N., Popova T., Popova A., Glotova O., Zotova O., Tikhomirova G.
Method Validation for Anticomplementary Activity of Human Immunoglobulin Drugs
Krivykh M., Kornilova O., Bunyatyan N., Paramonova E., Volkova R., Fadeikina O.
Validation of Methods and Procedures in Pharmacopoeial Monographs in the Framework of a Drug Standardization Program
Olefir Y., Sakanyan E., Luttseva A., Babeshina L., Shemeryankina T.
Method Development and Stress Degradation Profile of 5-Benzyl-1,3,4-Oxadiazole-2-Thiol Studied by UV Spectroscopy
Qamar S., Hussain K., Bukhari N., Shehzadi N., Islam M., Siddique S., Aziz-ur-Rehman
Validation of a Method of Measuring Mean Molecular Weight of Dextrans by Diffusion-Ordered Spectroscopy
Moiseev S., Kuz’mina N., Krylov V., Yashkir V., Merkulov V.
Selection of Standardization Parameters and Development of Quality Control Methods for Isoleucyl-Tryptophan Dipeptide Coordination Complex with Iron(II) (Timofer)
Bunyatyan N., Kholnazarov B., Olefir Y., Bobizoda G.
Validation of an Analytical HPLC Method for a New Diagnostic Octreotide Derivative for Neuroendocrine Tumors
Lar’kina M., Krivoshchekov S., Podrezova E., Bragina O., Chernov V., Nesterov E., Bodenko V., Belousov M., Yusubov M.
Development and Validation of a Quantitative Determination Technique for Phenibut in Microcapsules
Polkovnikova Y., Koryanova K., Slivkin A., Tul’skaya U., Senchenko S.
Development and Validation of a Quantitative Determination Method for the Antitubercular Drug PBTZ169 in Biological Media
Stepanova E., Barsegyan S., Makarenkova L., Chistyakov V.
GC-MS Determination of Mexiletine After Derivatization with N-Methyl-N-(Trimethylsilyl) Trifluoroacetamide in Pharmaceutical Formulatios and Comparison with HPLC Method
Yilmaz B., Nazik G., Kucukoglu K.
Validation of a Method for Measuring the Molar Substitution of Hydroxyethylstarches by 1H NMR Spectroscopy
Kuz’mina N., Moiseev S., Krylov V., Yashkir V., Merkulov V.
Validation of an Assay Procedure for Ormustine in a Liposomal Dosage Form
Bunyatyan N., Oborotova N., Nikolaeva L., Ignat’eva E., Yartseva I., Lantsova A., Prokof’ev A.
Development of a Sample-Preparation Procedure for Quantitative Determination of Lead in Sugars by Inductively Coupled-Plasma—Atomic-Emission Spectrometry (ICP-AES)
Olefir Y., Sakanyan E., Ladygina L., Shchukin V.
Quantitative Determination of Mycophenolic Acid in Human Blood Plasma by High-Performance Liquid Chromatography with Tandem Mass-Spectrometric Detection
Khokhlov A., Dzhurko Y., Shitov L., Kubeš V., Ryska M., Yaichkov I., Shitova A., Shabrov V., Miroshnikov A.
Determination of Cycloserine in Blood Plasma by HPLC/MS: Application to Bioequivalence Studies
Stepanova E., Ovcharov M., Barsegyan S., Chistyakov V.
Validation of Spectrophotometric Method for Determination of Thiamazole in Liquids by Dissolution Test for the Transdermal Form
Datkhayev U., Sakipova Z., Ustenova G., Zhakipbekov K., Kozhanova K., Kapsalyamova E., Datkayeva G., Ibadullayeva G., Sapakbay M., Bekenov K., Tulemissov S., Blatov R.
Validation of a Method for Assay of Trifluoroacetates in the Pharmaceutical Substance Glatiramer Acetate by 19F NMR Spectroscopy
Moiseev S., Kuz’mina N., Krylov V., Yashkir V., Merkulov V.
Development and Validation of an HPLC-UV Method for Anilocaine Determination in Blood Plasma
Ryzhikova V., Kursakov S., Belov V., Sevast’yanov V.
Validation of HPLC Method for Quantitative Determination of Gefitinib in Polymeric Nanoformulation
KS N., K G., Verma R., Ananthakrishna P., Kumar L.
UHPLC Method Development for Determining Sitagliptin and Dapagliflozin in Lipid-Based Self-Nanoemulsifying Systems as Combined Dose in Commercial Products and its Application to Pharmacokinetic Study of Dapagliflozin in Rats
Kazi M., Alqahtani A., Alsaadi B., Alkholief M., Alanazi F.
Development and Validation of a Stability-Indicating Liquid Chromatographic Method with Mass-Spectrometric Detection for the Analysis of Apixaban and Determination of Production Related Impurities
Arous B., Al-Mardini M.
Validation of an NMR-Spectroscopic Method for Authenticity Confirmation of Buserelin Acetate Pharmaceutical Substance
Kuz’mina N., Moiseev S., Krylov V., Deryabin A., Yashkir V., Merkulov V.
Development and Validation of an HPLC Method with Mass Spectrometric Detection for Quantitative Determination of Chlormadinone Acetate and Ethinyl Estradiol in Human Blood Plasma
Gil’deeva G., Belostotskii A., Sapozhnikova D.
Validation of a GC-MS Method for Quantitative Determination of Cyclohexanone by Oxidative Cleavage
Podrezova E., Lar’kina M., Yusubov M., Belousov M., Zamanova M., Krivoshchekov S.
Methods for Analytical Control of Darunavir Tablet Dosage Forms. Part II
Goizman M., Shimanovskii N., Shobolov D., Zotova O., Ermakova O., Tikhomirova G., Chernobrovkin M.
Development and Validation of a Method for Determination of a New Effective Inhibitor of Influenza Virus H1N1 in Blood Plasma
Sokolova A., Yarovaya O., Nefedov A., Salakhutdinov N.
LC Method Development and Validation for the Determination of Ropivacaine Hydrochloride in Bulk Drug and Pharmaceutical Formulations
Chigurupati S., Appala R., Selvarajan K., Khaw C., Teoh C., Batumanathan L., Mohammad J.
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