Legal implications for your Clinical Trials differ from country to country within the EU despite harmonization. We help you to shorten the way to find out, which regulatory documents apply to your country in question.
Please browse the table: It gives you an overview what documents are needed for Germany, The Netherlands, Belgium and Austria for submission of a Clinical Trial to the Ethics Committee (EC) and the Competent Authority (Reg). You can choose by country, Reg, EC and document.
>> open table
>> Click here to learn something about relevant timelines for your submission.