Clinical trial success depends upon the ability to properly communicate crucial data without the risk of misinterpretation. Clarity and accuracy are vital when writing all clinical trial documents.
Clear and accurate communications
Our team of expert medical writers comprises PhD-level scientists with excellent written communication skills. They have a diverse range of medical writing experience, as well as knowledge of regulatory documents over a wide spectrum of therapeutic areas.
Our teams deliver appropriately structured and targeted texts for clinical study reports, clinical trial protocols (CTPs), investigator brochures (IBs), efficacy and safety summaries, clinical overviews, publications, abstracts, posters and presentation, and narrative writing.
We offer:
- International Conference on Harmonization (ICH) compliant templates
- Experienced mediation of interdisciplinary teams to ensure clear and accurate documentation complying to scientific, ICH, regulatory and client standards
- Quick turnaround times with full quality control against source documents
- Readable, coherent, unambiguous, and navigable study documents, reducing review time and meeting the expectations of the entire clinical research team
Our experts work in partnership with you. They fulfill your requirements and will operate using either our template or a template devised by your team.
Why choose medical writing services from SGS?
We are recognized as the benchmark for quality and integrity in clinical research. Our experts deliver solutions that facilitate and expedite the success of your clinical trials.
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