Clinvigilant Research medical writers are experienced in both clinical and regulatory writing.
Our writers work closely with our biostatisticians and peer reviewers to ensure documents are complete and faithfully represent our high level of scientific rigor and patient care. Moreover, Clinvigilant Research’s highly collaborative approach ensures well-formed documents that take into account client preferences, local regulations, and guidelines.
Some of the documents routinely prepared by our writers include:
- Protocol synopsis documents
- Clinical trial protocols
- Informed Consent Forms (ICFs)
- Patient and staff diaries
- Clinical study reports