- Copy Editing
- Cross-language editing/proofreading
- Reference checking
- Online editing
- Stylistic editing
- Substantive and Structural Editing
- Technical editing of Articles
Business plans & presentations
Regulatory Documentation filings
Experience: pharmaceutical industry.
Strengths: well over 20 years in drug development generating and designing documents according to ICH, CTD, GCP, and GLP guidelines. Preference for electronic editing and reviews.
Specialties: FDA and Health Canada: Clinical and Nonclinical Study Reports and Protocols, CTA, IND, pre-IND, and NDA.