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Other RB norms

GF RB 01/2013:30202
GF RB 01/2013:30202
3.2.2. Plastic containers and closures for pharmaceutical use
GF RB 01/2013:30203
GF RB 01/2013:30203
3.2.3. Sterile plastic containers for human blood and its components
GF RB 01/2013:30204
GF RB 01/2013:30204
3.2.4. Empty sterile plasticized polyvinyl chloride containers for human blood and its components
GF RB 01/2013:30205
GF RB 01/2013:30205
3.2.5. Sterile plasticized polyvinyl chloride containers for human blood containing an anticoagulant solution
GF RB 01/2013:30206
GF RB 01/2013:30206
3.2.6. Kits for blood transfusion and blood components
GF RB 01/2013:30208
GF RB 01/2013:30208
3.2.8. Sterile Disposable Plastic Syringes
GF RB 01/2013:30209
GF RB 01/2013:30209
3.2.9. Rubber closures for containers intended for parenteral aqueous drugs, powders and lyophilized powders
GF RB 01/2013:40000
GF RB 01/2013:40000
4. Reagents
GF RB 01/2013:40100
GF RB 01/2013:40100
4.1. Reagents, reference solutions, buffer solutions
GF RB 01/2013:40101
GF RB 01/2013:40101
4.1.1. Reagents
GF RB 01/2013:40102
GF RB 01/2013:40102
4.1.2. Reference solutions for testing for the maximum content of impurities
GF RB 01/2013:40103
GF RB 01/2013:40103
4.1.3. Buffer solutions
GF RB 01/2013:40201
GF RB 01/2013:40201
4.2.1. Original Standard Substances for Titrated Solutions
GF RB 01/2013:40202
GF RB 01/2013:40202
4.2.2. Titrated solutions
GF RB 01/2013:50101
GF RB 01/2013:50101
5.1.1. Methods for the preparation of sterile products
GF RB 01/2013:50102
GF RB 01/2013:50102
5.1.2. Biological indicators of sterilization
GF RB 01/2013:50103
GF RB 01/2013:50103
5.1.3. The effectiveness of antimicrobial preservatives
GF RB 01/2013:50104
GF RB 01/2013:50104
5.1.4. Microbiological purity of non-sterile drugs and pharmaceutical substances
GF RB 01/2013:50105
GF RB 01/2013:50105
5.1.5. Application of the F0 concept in steam sterilization of aqueous solutions
GF RB 01/2013:50106
GF RB 01/2013:50106
5.1.6. Alternative methods of microbiological purity control
GF RB 01/2013:50107
GF RB 01/2013:50107
5.1.7. Viral safety
GF RB 01/2013:50108
GF RB 01/2013:50108
5.1.8. Microbiological purity of herbal medicines for internal use
GF RB 01/2013:50109
GF RB 01/2013:50109
5.1.9. Sterility Test Guidelines
GF RB 01/2013:50110
GF RB 01/2013:50110
5.1.10. Bacterial Endotoxin Test Guidelines
GF RB 01/2013:50201
GF RB 01/2013:50201
5.2.1. Common terminology in articles on biological products
GF RB 01/2013:50202
GF RB 01/2013:50202
5.2.2. Flocks of chickens that do not have specific pathogens and are used for the production and quality control of vaccines
GF RB 01/2013:50203
GF RB 01/2013:50203
5.2.3. Production cells for the production of vaccines for medical use
GF RB 01/2013:50208
GF RB 01/2013:50208
5.2.8. Reducing the risk of transmission of causative agents of spongy encephalopathy of animals when using medical drugs
GF RB 01/2013:50300
GF RB 01/2013:50300
5.3. Statistical analysis of the results of biological tests and tests
GF RB 01/2013:50500
GF RB 01/2013:50500
5.5. Alcohol tables
GF RB 01/2013:50600
GF RB 01/2013:50600
5.6. Quantitative determination of interferon
GF RB 01/2013:50700
GF RB 01/2013:50700
5.7. Table of the physical characteristics of the radionuclides referred to in the pharmacopoeia
GF RB 01/2013:50900
GF RB 01/2013:50900
5.9. Polymorphism
GF RB 01/2013:51000
GF RB 01/2013:51000
5.10. Control of impurities in substances for pharmaceutical use
GF RB 01/2013:51100
GF RB 01/2013:51100
5.11. Section "Description (Properties)" in private articles
GF RB 01/2013:51400
GF RB 01/2013:51400
5.14. Medicines for gene therapy for medical use
GF RB 01/2013:51600
GF RB 01/2013:51600
5.16. Crystallinity
GF RB 01/2013:51701
GF RB 01/2013:51701
5.17.1. Dissolution Test Recommendations
GF RB 01/2013:90001
GF RB 01/2013:90001
3.1.1.1. Materials based on plasticized polyvinyl chloride, used for the production of containers for human blood and its components
GF RB 01/2013:90002
GF RB 01/2013:90002
3.1.1.2. Materials based on plasticized polyvinyl chloride for tubes used in kits for blood transfusion and blood components
GF RB 01/2013:90003
GF RB 01/2013:90003
3.2.2.1. Plastic containers for water solutions for infusion
GF RB 01/2013:RB0002
GF RB 01/2013:RB0002
# Infusions, decoctions and teas
GF RB 01/2013:RB0003
GF RB 01/2013:RB0003
# Fees
GF RB 01/2013:RB0004
GF RB 01/2013:RB0004
# Medicinal plant raw materials whole or shredded packed up
GF RB 01/2013:RB0005
GF RB 01/2013:RB0005
# Registration requirements and rules for conducting bioavailability and bioequivalence studies of generic drugs
GF RB 01/2013:RB0006
GF RB 01/2013:RB0006
# Dragee
GF RB 01/2013:RB20550
GF RB 01/2013:RB20550
# 2.5.50. Titration in non-aqueous solvents
GF RB 01/2013:RB20750
GF RB 01/2013:RB20750
# 2.7.50. Determination of the biological activity of insulin

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