Aseptic simulation test for cytotoxic drug production in isolators

Author:

Savry Amandine1,Correard Florian1,Bennis Youssef1,Roubaud Sophie2,Gauthier-Villano Laurence3,Pisano Pascale4,Pourroy Bertrand5

Affiliation:

1. Oncopharma Unit, Pharmacy Department, La Timone University Teaching Hospital, Marseille, France.

2. Plein Ciel Clinic, Mougins, France.

3. Oncopharma Unit, Pharmacy Department, La Timone University Teaching Hospital.

4. Pharmacology Laboratory, Faculty of Pharmacy, Aix Marseille University, Marseille.

5. Oncopharma Unit, Pharmacy Department, La Timone University Teaching Hospital

Publisher

Oxford University Press (OUP)

Subject

Health Policy,Pharmacology

Reference16 articles.

1. Using a medium-fill simulation to evaluate the microbial contamination rate for USP medium-risk-level compounding;Trissel;Am J Health-Syst Pharm,2005

2. I.V. admixture contamination rates: traditional practice site versus a class 1000 cleanroom;Thomas;Am J Health-Syst Pharm,2005

3. ISOPP standards of practice. Safe handling of cytotoxics;International Society of Oncology Pharmacy Practitioners Standards Committee;J Oncol Pharm Pract,2007

4. National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention. NIOSH alert: preventing occupational exposure to antineoplastic and other hazardous drugs in health care settings. www.cdc.gov/niosh/docs/2004-165/pdfs/2004-165.pdf (accessed 2013 Dec 4).

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