We provide regulatory, scientific, and medical writing services to pharmaceutical and medical device companies, CROs, and research organizations. Below are some of the tasks we can assist you with:
- Document writing and editing for regulatory submissions. For example, eCTD modules in IND, NDA, and BLA submissions. Our medical writers will serve as an integrated member of your team, collaborating with other team members across multiple functions
- Surveys, outreach materials, and educational brochures for lay persons or professionals
- Meeting minutes for workshops and academic conferences
- Program reports for collaborative research
Our medical writers are qualified by their education, training, and years of experience in the fields of clinical trials and/or medical writing.