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Research Article

Validation of Cleaning Procedures for Highly Potent Drugs. II. Bisnafide

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Pages 471-476 | Received 21 Aug 1997, Accepted 21 Jan 1998, Published online: 27 Sep 2008

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Antje Böhlandt, Svenja Groeneveld, Elke Fischer & Rudolf Schierl. (2015) Cleaning Efficiencies of Three Cleaning Agents on Four Different Surfaces after Contamination by Gemcitabine and 5-fluorouracile. Journal of Occupational and Environmental Hygiene 12:6, pages 384-392.
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Zoran Bubnič, Uroš Urleb, Katjuša Kreft & Marjan Veber. (2011) The application of atomic absorption spectrometry for the determination of residual active pharmaceutical ingredients in cleaning validation samples. Drug Development and Industrial Pharmacy 37:3, pages 281-289.
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Articles from other publishers (7)

B.W. Pack, S. Stithit & W. Chen. 2017. Developing Solid Oral Dosage Forms. Developing Solid Oral Dosage Forms 653 676 .
Laetitia Minh Mai Lê, Pierre Alain Jolivot, Hassane Sadou Yayé, André Rieutord, Agnès Bellanger, Dominique Pradeau, Séverine Barbault-Foucher & Eric Caudron. (2012) Effectiveness of cleaning of workplace cytotoxic surface. International Archives of Occupational and Environmental Health 86:3, pages 333-341.
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. (2010) Pilot Study Comparing the Efficacy of Two Cleaning Techniques in Reducing Environmental Contamination with Cyclophosphamide. The Annals of Occupational Hygiene.
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Brian W. Pack. 2009. Formulation and Analytical Development for Low‐Dose Oral Drug Products. Formulation and Analytical Development for Low‐Dose Oral Drug Products 345 380 .
Brian W. Pack, Suchinda Stithit, Lisa Ray, Wei Chen, Jack Y. Zheng & Richard Hwang. 2009. Developing Solid Oral Dosage Forms. Developing Solid Oral Dosage Forms 577 597 .
Li Liu & Brian W. Pack. (2007) Cleaning verification assays for highly potent compounds by high performance liquid chromatography mass spectrometry: Strategy, validation, and long-term performance. Journal of Pharmaceutical and Biomedical Analysis 43:4, pages 1206-1212.
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Emma L. Simmonds, W. John Lough & Martin R. Gray. (2006) Evaluation of LC–MS for the analysis of cleaning verification samples. Journal of Pharmaceutical and Biomedical Analysis 40:3, pages 631-638.
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