Drafting clear, concise and accurate scientific documents requires technical training and enough regulatory and scientific knowledge to ensure that these documents are accepted by Health Authorities as well as by main journals and cutting-edge media in biomedical environment. In addition, previous knowledge of legal regulations and the specific therapeutic areas (Final Results Report, Abstracts, Posters for conferences, Protocols, Patient Information and Informed Consent Forms, etc.) is required.
Having participated in a large number of clinical studies of different pathologies (oncology, hematology, endocrinology, gynecology, cardiovascular, neurology, etc.) and a large number of clients from different fields (pharmaceutical and medical device industry , independent researchers and biotechnology companies), Experior has the experience required to draft those scientific texts and documents, including but not limited to Protocols, Patient Information and Informed Consent Forms, and Clinical Study Reports (CSR). All the reports related to the dissemination of results generated by Experior are made following the ICH guidelines (ICH E3 Structure and Content of Clinical Study Reports) to ensure that they meet the internationally recognized standards.
Experior offers a customized medical writing service within very tight deadlines. In addition, we are familiar with different writing styles due to our wide range of clients.
Patient Information and Informed Consent Forms drafted
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