Acadustri provides expert medical writing solutions for the pharmaceutical industry and academic research institutions that collaborate with the industry in early-stage clinical development. Our industry experience and extensive medical writing credentials mean we are ideally placed to offer authoritative guidance on document content and structure, in addition to end-to-end writing for all stages of drug development. Acadustri's position as an experienced industry leader in the preparation of safety documents means that we are well placed to both write and provide guidance regarding the increased scientific complexity of PSURs and RMPs since implementation of the Good Pharmacovigilance Practices guidelines. We also have expertise in the preparation of clinical/regulatory documents, articles for publication in peer-reviewed journals, as well as congress and training materials.