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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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April 30, 2008: BASF sells its Shreveport site and related contract manufacturing business to Dr. Reddy's Laboratories (english, deutsch) January 18, 2008: BASF appoints Folker Ruchatz as head of its custom synthesis business (english, deutsch)
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