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EudraPharm FAQ |
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This information can be viewed on the About EudraPharm page. |
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♦ Click on the blue diamond underneath your desired language to open a Product-Information Document related to the product you are currently viewing. The Product-Information Documents can contain the following information: Labelling, Package Leaflet and Summary of Product Characteristics. |
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♦ The diamond icon is greyed out if a Product-Information Document is not available for the language listed above the grey diamond. |
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You can find a product in EudraPharm by using any of the options listed below: |
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First find the product(s) using any of the options listed above. |
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Then click on the name of the product that you are interested in to display the product information. |
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Click here for further details about product information. |
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A Product-Information Document is a group of documents containing all of the information regarding the way a medicinal product may be used and how it should be labelled. The group of documents includes: |
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Click the blue diamond ♦ on the product information page to open a Product-Information Document related to the product you are currently viewing. Note that Product-Information Documents may not be available for all products in EudraPharm. |
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Can I view information about side effects, indication and usage? |
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This information is available in the Product-Information Documents (see question above). |
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Click here to find out what a maximum residue limit is. |
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Where can I find the definitions for terminology used in EudraPharm? |
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This information can be viewed in the Glossary page. |
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This information can be viewed in the EudraPharm Notices page. |
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Where can I find information about JavaScript and EudraPharm? |
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This information can be viewed in the EudraPharm Notices page. |
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Can I find out if a product is sold in a particular country? |
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EudraPharm does not currently contain any marketing information. |
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Where can I find details about Copyright, Terms and Conditions and Privacy Policy? |
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You can find all the legal details on the EudraPharm Notices page. |
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The Portable Document Format (PDF) is an electronic file format developed by Adobe Systems Inc. as part of their Acrobat® family of software. If you do not have a version of Acrobat installed, you will need to download Adobe® Reader® to open and view PDF files. Adobe® Reader® is available to users at no cost. |
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Click this link http://www.adobe.com/prodindex/acrobat/readstep2.html to download the software from the Adobe website. |
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EudraPharm is best viewed at a screen resolution of 1024 x 768 pixels. However, you can still view all the information in lower resolutions. Remember to scroll to the right when viewing EudraPharm pages in lower screen resolutions, as there may well be information in the browser window that does not appear on screen. |
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Click here for details on how to contact the EudraPharm Helpdesk. |