Effectively leading the preparation and delivery of medical documents is an art. Our medical writers work closely with our customers, for example by leading key meetings and ensuring all the required quality controls are in place. Every document undergoes thorough scientific, statistical and editorial review.
Our medical writers have a wide breadth of knowledge and experience drawn from experiences in the pharmaceutical industry, other CROs and in academia. This experience helps us consistently meet timelines for the development of clinical documentation – with high-quality writing that reduces the need for additional review and re-work, saving you time and money.
Wide range of services
> Clinical trial documents (Protocols, Study Reports)
> Development documents
For anything not listed here, please contact us and we will be happy to evaluate.
Praise for a recent delivery (CSR for a Phase III Oncology program)
“It was so easy to complete this project with you. We had to rely on your expertise and leadership to bring this last effort to conclusion. And you could bring all the pieces together – we could just SEE it!”