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How can we help you?

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.

Founded by the author of ‘Pharmacovigilance Medical Writing: A Good Practice Guide’, Acadustri is an industry leader in the provision of pharmacovigilance medical writing services and is fast becoming the business partner of choice for the preparation of safety documents.

What our clients say

  • "Justina wrote several clinical study reports for us and we would not hesitate to hire her services again. The work she produced was of high quality, delivered on time and she was easy to work with.”

    Associate Director, Clinical Submissions Writing, UK-Based Biopharm Company

  • "....has shown great flexibility and expertise in regulatory documents and beyond....has continuously demonstrated strong writing and project management skills, and has a great ability to step in quickly and efficiently."

    CK, Associate Director of Medical Writing, Biogen Idec, USA

  • “Consistently reliable in providing quality documents regardless of the deliverable type requested. Always willing to share expertise and provide improvement opportunities to enhance the document output.”

    Salvatore Curti, Vice President and Head Drug Safety Operations & Mari Welke, Head of Aggregate Reporting, UCB BioSciences Inc.