We work with you as integral team members, providing proactive project planning, document creation, and document life-cycle management, with a commitment to timeliness and excellence. We have been privileged to serve over 65 pharmaceutical and biotechnology companies of all sizes, worldwide, for over 20 years. If you are looking to produce the highest-quality documents on-time and in-budget, contact us.

We have partnered with AI developers to create initial drafts of clinical study documents in just 5 days. Using our AI-powered medical writing tool, we generate your clinical study protocol, informed consent form, study procedures manuals, and start-up checklists simultaneously.