Comprehensive writing solutions for clinical trials to deliver accurate, clear and submission-ready documents.
Medical Writing Services
Our team of methodologists, epidemiologists, biostatistician, clinical trial managers and social scientists have vast experience in global health research and clinical trials across Sub-Saharan Africa. Our success in medical writing lies in our ability to engage with all trial stakeholders early on to identify implementation challenges and incorporate them into the protocol development. Further, we employ innovative, context relevant community engagement strategies in order to have a truly efficient and effective trial for participants and acceptable for our communities and country regulatory authorities.
Our Medical Writing Services are:
- Scientific literature review and research gap analysis
- Protocol development (full protocol development)
- Informed consent sheet/form (ICF) (paper form and electronic form)
- Patient facing tools development
- Standard Operating Procedures development
- Investigator’s Brochure creation
- Community Engagement Strategy
- Clinical study reports creation (paper form, web application format)
- Medical review of study documents and materials (protocols, CRF, data, listings, reports)
- Medical writing for abstract and manuscript
- Support and assistance with conference/journal submission
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