Savio understands the importance of regulatory Medical Writing in Clinical Research that is written in a clear and precise manner which is easily understood by IRB, FDA and any other reviewers.

Our qualified regulatory medical writing services help you in composing well-written regulatory documents and ensure that your clinical trial protocol is reviewed; edited and proofread properly that helps you save time and money. Savio medical writers work closely with statistical, medical regulatory and data management team to deliver the meticulously precise document to the highest ethical and scientific industry standards.

Clinical development plans Protocols

Clinical study reports

Abstracts, manuscripts, and journal articles

Informed consent forms

Investigator brochures and annual updates

Medical and scientific literature reviews