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Quality and regulatory
In order to use an excipient you need to obtain a significant amount of data about the manufacturer and the excipient itself. Contact us to receive standardised information from our regulatory and quality support package (e.g. basic schematics of our production process, so-called Process Flow Sheet).
The documents should not be viewed as a replacement for audits. DFE Pharma has chosen this way of information-sharing in order to provide information to the user as quickly as possible. If you wish to audit one of our facilities, please contact your DFE Pharma sales representative.
Because our PDF QAR documents are technically certified, you may experience difficulties when opening them in a browser. Save the PDF file first and then open the PDF file in a standard PDF reader (e.g. Adobe Reader).
If you have troubles opening the documents please download Adobe Acrobat Reader here.