– Informed Consent Forms, Patient diaries, and patient information
– Patient Safety Narratives
– Regulatory documents, responses, and regulatory submission support
Our Medical Writers are experienced in the development of protocols, IBs, ICFs and reports of any level of complexity within different therapeutic fields.
X7 also has a number of translators as part of our trial support system. During the registration process, we will manage the preparation and submission of the dossier, the supervision of the registration process, as well as communication with the authorities and translation of product texts into local languages.