Research Paper (929)

  • Longterm physicochemical stability of ready-to-administer human insulin injection solutions 1 I.U./mL in 50 mL plastic syringes
    Longterm physicochemical stability of ready-to-administer human insulin injection solutions 1 I.U./mL in 50 mL plastic syringes

    Erdnüß Frank

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  • Long-term stability of ready-to-use epinephrine 0.02 mg/mL injection solution in 50 mL glass vials
    Long-term stability of ready-to-use epinephrine 0.02 mg/mL injection solution in 50 mL glass vials

    Heeb Rita Marina

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  • Physicochemical stability of 20 mg/mL amiodarone hydrochloride oral suspension in SyrSpend® SF PH4 (liquid)
    Physicochemical stability of 20 mg/mL amiodarone hydrochloride oral suspension in SyrSpend® SF PH4 (liquid)

    Adoum Anissa

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  • Stability of voriconazole 10 mg/mL ophthalmic solution during 90 days
    Stability of voriconazole 10 mg/mL ophthalmic solution during 90 days

    Khan Aasfa

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  • Y-site compatibility of intravenous medications commonly used in intensive care units: laboratory tests on 75 mixtures involving nine main drugs
    Y-site compatibility of intravenous medications commonly used in intensive care units: laboratory tests on 75 mixtures involving nine main drugs

    Ayari Gillian

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  • Physicochemical stability of azacitidine suspensions at 25 mg/mL in polypropylene syringes stored under different conditions of storage
    Physicochemical stability of azacitidine suspensions at 25 mg/mL in polypropylene syringes stored under different conditions of storage

    Trambloy Quentin

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  • Evaluation of the hazardous drug surface contamination in pharmacy compounding and administration clinical setting after adoption of standardized cleaning workflow and a closed system transfer device
    Evaluation of the hazardous drug surface contamination in pharmacy compounding and administration clinical setting after adoption of standardized cleaning workflow and a closed system transfer device

    Bishay Sally

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  • Physicochemical stability of Cabazitaxel Zentiva® solution in vials after opening and diluted solutions in three infusion bags
    Physicochemical stability of Cabazitaxel Zentiva® solution in vials after opening and diluted solutions in three infusion bags

    D’Huart Elise

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  • An exploratory study of a simplified approach to evaluate drug solubility in milk related vehicles
    An exploratory study of a simplified approach to evaluate drug solubility in milk related vehicles

    Li Sean

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  • Use of a liquid chromatography-tandem mass spectrometry method to assess the concentration of epinephrine, norepinephrine, and phenylephrine stored in plastic syringes
    Use of a liquid chromatography-tandem mass spectrometry method to assess the concentration of epinephrine, norepinephrine, and phenylephrine stored in plastic syringes

    Cohen Alejandro M.

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  • Air contamination, syringe contamination, and cross-contamination when using an automatic compounding device for sensitizing drugs
    Air contamination, syringe contamination, and cross-contamination when using an automatic compounding device for sensitizing drugs

    Sessink Paul

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  • Long term physicochemical stability study of novel ophthalmic formulations combining ceftazidime and vancomycin with and without cyclodextrins
    Long term physicochemical stability study of novel ophthalmic formulations combining ceftazidime and vancomycin with and without cyclodextrins

    Plaidy Pauline

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  • Physicochemical stability study of a biosimilar of Bevacizumab in vials and after dilution in 0.9% NaCl in polyolefin intravenous bags
    Physicochemical stability study of a biosimilar of Bevacizumab in vials and after dilution in 0.9% NaCl in polyolefin intravenous bags

    Vieillard Victoire

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  • Physicochemical stability of urea-containing Mitomycin C preparations in glass vials (1.0 mg/mL) and plastic syringes (2.0, 0.4, 0.2 mg/mL)
    Physicochemical stability of urea-containing Mitomycin C preparations in glass vials (1.0 mg/mL) and plastic syringes (2.0, 0.4, 0.2 mg/mL)

    Almasi Jannik

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  • Assessment of the relevance of osmolality measurement as a criterion for the stability of solutions
    Assessment of the relevance of osmolality measurement as a criterion for the stability of solutions

    Vigneron Jean

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  • Physicochemical stability of durvalumab (Imfinzi®) concentrate for solution in original vials after first opening
    Physicochemical stability of durvalumab (Imfinzi®) concentrate for solution in original vials after first opening

    Almasi Jannik

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  • Semi-automatic COVID-19 vaccine preparation for upscaling of vaccination: a descriptive study
    Semi-automatic COVID-19 vaccine preparation for upscaling of vaccination: a descriptive study

    van der Nat Denise J.

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  • Lyophilization-free proliposomes for sustained release oral delivery of hydrophobic drug (cinnarazine): a comparative study
    Lyophilization-free proliposomes for sustained release oral delivery of hydrophobic drug (cinnarazine): a comparative study

    Abu Abed Omar S.

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  • Efficacy of two intensive decontamination protocols and their effects after 30 days on environmental contamination by cyclophosphamide
    Efficacy of two intensive decontamination protocols and their effects after 30 days on environmental contamination by cyclophosphamide

    Delafoy Clémence

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  • Fifth DSRG symposium at CHU UCL Namur, 18/10/2019. “Centralization of injectables and robotization”
    Fifth DSRG symposium at CHU UCL Namur, 18/10/2019. “Centralization of injectables and robotization”

    Hecq Jean-Daniel

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  • Vial coring and fragmentation incidence after angled penetration of rubber stoppers with single-use hypodermic needles
    Vial coring and fragmentation incidence after angled penetration of rubber stoppers with single-use hypodermic needles

    Rase Marissa

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  • Physicochemical stability of human insulin 1 I.U./mL infusion solution in 50 mL polypropylene syringes
    Physicochemical stability of human insulin 1 I.U./mL infusion solution in 50 mL polypropylene syringes

    Mohr André

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  • New liquid oral formulations of hydroxychloroquine: a physicochemical stability study
    New liquid oral formulations of hydroxychloroquine: a physicochemical stability study

    Lebreton Vincent

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  • Risks associated with the evolution in the compounding process of parenteral nutrition solutions: use of the “FMECA” method
    Risks associated with the evolution in the compounding process of parenteral nutrition solutions: use of the “FMECA” method

    Dozias Gautier

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  • Use and impact of technology-assisted workflow (TAWF) systems for drug compounding in pharmacy practice: a scoping literature review
    Use and impact of technology-assisted workflow (TAWF) systems for drug compounding in pharmacy practice: a scoping literature review

    Farcy Elisabeth

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  • Antimicrobial preservation efficacy of liquid glucose and liquid maltitol syrups with and without 0.1% sorbic acid
    Antimicrobial preservation efficacy of liquid glucose and liquid maltitol syrups with and without 0.1% sorbic acid

    Carpentier Thomas

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  • Risk management in an anticancer drug preparation unit: use of Preliminary Risk Analysis method and application to the preparation process
    Risk management in an anticancer drug preparation unit: use of Preliminary Risk Analysis method and application to the preparation process

    Gagaille Marie-Pauline

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  • The future of care and clinical research in autism — recommendations from the 2021 Lancet Commission
    The future of care and clinical research in autism — recommendations from the 2021 Lancet Commission

    Yu Xiang

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  • Spontaneous pain as a challenge of research and management in chronic pain
    Spontaneous pain as a challenge of research and management in chronic pain

    Ma Longyu

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  • Crosstalk between bone and other organs
    Crosstalk between bone and other organs

    Yuan Wanqiong

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