- Protocol synopsis for Phases I to IV studies
- Study Protocols for Phases I to IV studies
- Investigator Brochures
- Study reference manuals
- Informed consent documents (ICD)
- Patient information sheet(PIS)
- Clinical Study Reports (CSRs)
- Clinical evaluation report (CER) Writing
- Clinical and non clinical sections of the CTD
- Summaries and overviews for EU and US
- Patient Safety Narratives
Medical and Scientific writing
Clinical research benefits greatly from the expertise of our medical and scientific writing staff. To produce accurate, timely, and cost-effective outputs that meet the highest quality and scientific requirements, our Medical Writers collaborate closely with the safety, biostatistics, medical affairs, and data management teams.
Our extensive knowledge comes from working for clinical research organizations and the pharmaceutical business. We will perform extensive scientific, statistical, editorial, and quality control reviews on every paper we produce.
In addition to scientific communications and medical writing consulting, we offer clinical and non-clinical writing services.
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Clinical and non clinical writing
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Scientific communications
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