INFORMATION PROVIDING CENTRE HOLLAND
The core-business of IPC-Holland is the production of Nonclinical (Module 2.4) and Clinical Overviews (Module 2.5), which form part of the presently required Common Technical Document (CTD), necessary for the registration of medicinal products in the European Union. Both our clients as well as the Dutch Medicines Evaluation Board (MEB) have been very satisfied with our reports due to their high quality. Besides Nonclinical and Clinical Overviews, we also draw up Expert Reports (part IC2 and IC3), Summaries of Product Characteristics, package leaflets and Periodic Safety Update Reports (PSURs). We also provide translations from English to Dutch and vice versa of various documents.
Because the market changes continuously, the services that IPC-Holland offers change as well. Therefore, if you do not find what you are looking for in this brochure, please do not hesitate to contact us. We may find a solution for your problem just as well.
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