Clinvigilant Research medical writers are experienced in both clinical and regulatory writing techniques to provide concisely written documents that exceed client expectations.
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.
We have developed several templates of protocols, ICFs, patient diaries, and other deliverables for various models. These vetted templates allow us to prepare important documents with high quality and fast turnaround.
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