dicentra’s team of medical experts have years of experience writing regulatory documents for NHP and dietary supplement applications to regulatory bodies worldwide. Our team also has experience in over 450 clinical trials and have 200+ publications in scientific journals.
Clinical Trial Documentation Support Including:
- Protocol Design & Development
- Informed Consent Forms
- Clinical Study Reports
- Preparation of electronic Common Technical Documents
- Clinical Trial Site Information Forms
Clinical Trial Documentation Support Including:
- New Drug Submissions
- New Drug Authorizations
- Clinical Trial Applications
- Supplement to a New Drug Submission
- Drug Identification Number
Medical Writing Support Including:
- Abstracts
- Research Posters
- White Papers
- Scientific Journal Articles
- Slide Decks for Conferences & Meetings
Learn more about how dicentra‘s scientific/medical writing services can help you meet your clinical research goals