Our scientific-minded team has several years of experience in preparing regulatory and research-related documents including early- and late-phase trial protocols, scientific conference abstracts, presentations, scientific-journal manuscripts, clinical study reports (CSRs), investigator’s brochures, clinical development dossiers, research product manuals, clinical laboratory manuals, patient´s questionnaires or informative materials, and informed consent forms, in accordance with Good Clinical Practices (GCP) regulations.
High-quality scientific writing, in any medical specialty, following regulatory guidelines for the generation of essential documents that support clinical research in order to fulfill requirements of different regulatory agencies.
