19 results on '"Hama, Koji"'
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2. Verification of Maintaining Sterility in Vial due to Different Storage Requirements for Reuse of Single-dose Vials
3. Study on Safety of Reusing the Residual Drug Solution in a Single-dose Vial at the Time of Needle Puncture
4. Verification of the Effect of a Simplified Washing Procedure with Water, Sodium Hypochlorite or Ozone Water on the Decontamination of Intentionally Contaminated Vial Surfaces by Anti-neoplastic Drugs
5. Evaluation of Decontamination Methods of Antineoplastic Drugs Using Ozone Water and Sodium Hypochlorite
6. Verification of External Surface Contamination of Japanese 5-fluorouracil Vials and Removal of Contamination by Washing the Vials
7. Microbiological Challenge Test of Contamination Caused by Using the PhaSeal System
8. The Evaluation of Comprehensive Countermeasures to Reduce Occupational Exposure to Anticancer Drugs during Preparation and Administration
9. Verification of surface contamination of Japanese cyclophosphamide vials and an example of exposure by handling
10. Comprehensive Evaluation of Cyclophosphamide Wipe Test Using Commercial Laboratory in Japan
11. Investigation on residual-related error and the effect of solution properties using protective devices for the reconstitution of cytotoxic agents in actual situations
12. Compatibility Assessment of Closed-system Device "PhaSeal SOLUS" and Antineoplastic-agent Vials
13. Dispensing Environment Factors Influencing Exposure to Powdered Drugs-Significance in Preparation of Antineoplastic Agents-
14. Economic Benefits of Using Residual Anticancer Agents Based on Medical Fee Calculation Procedure And Microbiological Considerations
15. Introduction of Measures to Prevent Errors in Preparation of Anticancer Agents Using Preparation Support Information-Development of System for Use with Injection Labels-
16. Investigation of Inquiries on Ambulatory Cancer Chemotherapy Prescriptions
17. Verification of surface contamination of Japanese cyclophosphamide vials and an example of exposure by handling.
18. Investigation on residual-related error and the effect of solution properties using protective devices for the reconstitution of cytotoxic agents in actual situations.
19. [Consideration on Expiration Days Setting for the Introduction of Drug Vial Optimization].
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