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Production and Preparation
PP-041
CENTRALISED NON-HAZARDOUS INTRAVENOUS COMPOUNDING: FROM THEORY TO CLINICAL PRACTICE
PP-057
PHARMACEUTICAL QUALIFICATION OF BIOINVERT® 200, AN ENZYME SUBSTITUTE TO SUCRAID®
PP-021
EVALUATION OF THE SURFACE CONTAMINATION IN A CHEMOTHERAPY PREPARATION UNIT BEFORE A PROCESS CHANGE
PP-012
CONSERVING COLD CHAIN COMPLIANCE IN THE RECONSTITUTION OF VIDAZA® IN ISOLATORS
PP-058
EVOLUTION OF THE PAEDIATRIC PARENTERAL NUTRITION BAG PRESCRIPTIONS FURTHER TO THE NUMETAH (THREE CHAMBER BAG) MARKETING
PP-054
STABILITY STUDY OF 100 MG/ML PAEDIATRIC PYRAZINAMIDE ORAL SUSPENSION IN SYRSPEND
PP-051
CYTOTOXIC CONTAMINATION RESEARCH IN A CENTRALISED CYTOTOXIC UNIT TO IMPROVE PROFESSIONAL PRACTICES
PP-049
IMPACT OF IMMUNOTHERAPY ARRIVAL IN CHEMOTHERAPY PRODUCTION UNITS : RETROSPECTIVE STUDY AND PROJECTION WITH ANTI-PD-1 AGENTS
PP-048
ANTINEOPLASIC: ANTICIPATED PREPARATIONS OR LONGER OPENING HOURS?
PP-047
AUTOMATED INTRAVENOUS CHEMOTHERAPY WORKFLOW: THE ADDED BENEFIT TO REDUCE POTENTIAL MEDICATION ERRORS
PP-046
A STABILITY INDICATING HPLC-UV METHOD FOR QUANTIFICATION OF SIMVASTATIN AND DETECTION OF ITS IMPURITIES IN ORAL CAPSULES
PP-044
STABILITY OF 50 AND 100μG/0.1ML INTRAOCULAR SOLUTIONS OF VORICONAZOLE AT 2-8°C
PP-041
CENTRALISED NON-HAZARDOUS INTRAVENOUS COMPOUNDING: FROM THEORY TO CLINICAL PRACTICE
PP-040
EVALUATION OF THERAPY MANAGEMENT FOR PREVENTION OF CHEMOTHERAPY INDUCED NAUSEA AND VOMITING IN A CENTRALISED INTRAVENOUS COMPOUNDING FACILITY
PP-039
IMPACT OF MASKING OF METHYLPHENIDATE DISSOLUTION FOR OVER ENCAPSULATED CAPSULES OF RITALIN LA 10 MG
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