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- DMF TECHNOFLEX Drug Master File n° 19057 at US FDA is available for all TECHNOFLEX’ standard ranges of products. - VALIDATION TECHNOFLEX’ range of products have been validated in compliance with the following regulations: - ISO 15747-2003 - PE 3.2.2.1 - USP Class VI and 661 - DOCUMENTATION Data and documents are provided for regulatory filing (European CTD, NDA and ANDA) for TECHNOFLEX’ customers. |
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TECHNOFLEX ZA de Bassilour - 64210 BIDART - France Internet : www.technoflex.net
Tél: + 33 (0) 559 54 66 66 - Fax: + 33 (0) 559 54 90 06 - E-mail: info@technoflex.net Dernière mise à jour : 03-06-2008 |
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