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Safe and sure quality.
Quality is our watchword – and not just because the production of pharmaceuticals is subject to strict regulations. Our active ingredients, excipients and exclusive ingredients are produced by trained and experienced BASF staff in line with the highest quality requirements. All our sites fulfill quality standard ISO 9001 as well as the internationally valid regulations of current Good Manufacturing Practice (cGMP). Our production sites are regularly inspected by national and international supervisory authorities, for example by the American Food and Drug Administration (FDA), and are open for customer audits.
Our employees in Quality Management guarantee the highest quality for BASF products at all sites worldwide. They ensure the implementation of uniform standards and processes as well as compliance with all relevant statutory and regulatory requirements. Thanks to continuous investments in our Quality Management system we can meet these regulations as well as the most demanding customer requirements.
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March 2, 2010: BASF showcases its expertise at the 7th World Meeting on Pharmaceutics, Biopharmaceutic and Pharmaceutical Technology in Malta (english) February 10, 2010: BASF has joined forces with GEA Niro in cGMP spray drying for
custom synthesis pharma production (english, deutsch) December 3, 2009: New packaging for an all-round talent from BASF - Polyvinylpyrrolidone (english) November 5, 2009: Color-perfect, efficient, environment-friendly tablet
production (english) October 13, 2009: Soluplus® – for effective drug delivery (english) October 12, 2009: BASF showcases expertise at the CPhI worldwide in Madrid (english)
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