Services
Regulatory Writing
I help pharma, biotech, and medical device companies and CROs write clear, precise, and submission-ready regulatory documents.
- Clinical/Non-Clinical Study Protocol
- Clinical/Non-Clinical Study Report
- Investigator's Brochure
- Case Report Form
- Case Narrative
- Clinical Evaluation Report for class I and II devices
Medical Communications
I enjoy writing medical communications documents that are tailored to the target audience for pharma companies and medical communication agencies.
- Manuscripts, including reviews
- Systematic Literuture reviews
- Presentations for KOLs, board meetings
- Congress materials ( abstracts, posters, presentations)
- Plain language summaries
Others
- Advisory board meetings (Presentation slides, executive summaries, reports, KOL interviews)
- QC of regulatory documents
- Editing and proofreading manuscripts
- Blogs