Medical Writing
Pharmaceutical
- Clinical Study Protocols
- Clinical Study Reports
- Investigator’s Brochures
- Patient Information Leaflets
- Manuscripts for Publication
- Abstracts and Conference Posters
- Case Study Reports
- Literature Reviews
- Clinical Trial Registration Documents
- Patient Consent Forms
- Common Technical Document (CTD) Modules
- Periodic Safety Update Reports (PSURs)
- Periodic Benefit-Risk Evaluation Reports (PBRERs)
- Risk Management Plans (RMPs)
- Summary of Product Characteristics (SmPC)
- Clinical Overview and Summaries
- Regulatory Submission Documents
Medical Device
- Clinical Evaluation Reports
- Clinical Investigation Plans
- Clinical Study Reports
- Investigator’s Brochures
- Patient Information Leaflets
- Manuscripts for Publication
- Abstracts and Conference Posters
- Case Study Reports
- Literature Reviews
- Patient Consent Forms
- Technical File Documentation
- Design Dossiers
- Summary Technical Documentation
- Pre-Market Approval Applications
- 510(k) Submissions
- Risk Management Files
- Post-Market Surveillance Reports
- Periodic Safety Update Reports
- Clinical Evaluation Plans
- Regulatory Submission Documents
