Teva Pharmaceutical
- PharmAssess™ GMP Audit
About Teva Pharmaceutical Industries Ltd
Teva Pharmaceutical Industries Ltd. is a global pharmaceutical company specializing in the development, production and marketing of generic and proprietary branded pharmaceuticals as well as active pharmaceutical ingredients. Teva is among the top 20 pharmaceutical companies and among the largest generic pharmaceutical companies in the world.
In January , 2004, Sicor became a wholly-owned subsidiary of Teva, bringing together two premier generic pharmaceutical companies, combining Teva's successful oral dose generic drugs franchise with Sicor's leading generic injectable business. In addition, both the Active Pharmaceutical Ingredients (API) businesses and Sicor's biogenerics capabilities will enhance and expand the combined company's product offerings. (Note: "Sicor" was renamed "Teva Parenteral Medicines, Inc." in 2007.)
About the Audit
The audit of the Teva - Sicor site was performed on 9 April 2008. The Report includes photographs and is 33 pages long, excluding appendices. Including appendices the Report is 52 pages long.
The Audit Report provides information on the site facilities and covers a wide range of materials, including;
Beclomethasone Dipropionate, Budesonide, Clobetasolo Propionato, Desoximetasone, Doxorubicina Cloridrato, Epirubicina Cloridrato, Etoposide, Idarubicina Cloridrato, Methylprednisolone Sodium Succinate, Metilprednisolone Emisuccinato, Norgestimate, Pixantrone.
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Ad-Hoc Audit Requirements
Please note that if there are other audits that you require, which are not in the PharmAssess Section of this website, please contact us to discuss your audit requirements, which we can undertake on your behalf.
Rephine has an ongoing programme of audits which is being constantly updated. If an audit you require is not on the list of those available, please contact the Rephine office to establish whether it is in the programme to be done or how it can be fitted in to the programme.
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Further Information
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