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| Issue |
Title |
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| Vol 13, No 3 (2023) |
Recommendations for the Contents of a Product Specification File: Related Substances (HPLC) |
Abstract
PDF (Rus)
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|
O. A. Vaganova, A. A. Natykan |
| |
| Vol 12, No 3 (2022) |
Control of Residual Organic Solvents in Active Substances |
Abstract
PDF (Rus)
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|
O. A. Matveeva |
| |
| Vol 12, No 3 (2022) |
Practical Aspects of Processing and Interpretation of the Results of Microbiological Analysis of the Quality of Non-Sterile Medicines |
Abstract
PDF (Rus)
|
|
O. V. Gunar |
| |
| Vol 12, No 2 (2022) |
Recommendations on Describing the Requirements for Microbiological Quality and Sterility of Medicinal Products |
Abstract
PDF (Rus)
|
|
O. V. Gunar |
| |
| Vol 12, No 2 (2022) |
Recommendations for Choosing a Test Dose for Abnormal Toxicity Testing |
Abstract
PDF (Rus)
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|
E. O. Stepanuk, N. P. Neugodova |
| |
| Vol 12, No 1 (2022) |
Methodology for Calculating Bacterial Endotoxin Limits |
Abstract
PDF (Rus)
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|
O. V. Shapovalova, N. P. Neugodova |
| |
| Vol 11, No 4 (2021) |
Recommendations for the Contents of the “Glycan Profile” Part of a Product Specification File |
Abstract
PDF (Rus)
|
|
O. A. Vaganova |
| |
| Vol 11, No 4 (2021) |
Recommendations for the Contents of the “Peptide Mapping” Part of a Product Specification File |
Abstract
PDF (Rus)
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|
O. A. Vaganova |
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