Medical Writing
ERIC's Medical Writing Services
At ERIC, our medical writers collaborate with medical teams and statisticians to create accurate, regulatory-compliant clinical study reports (CSRs) while adhering to strict timelines. We follow ICH E3 guidelines or sponsor-specific formats to ensure clarity and compliance.
We also support eCTD submissions and provide abstract, poster, and manuscript preparation, helping sponsors effectively present their study findings.
Services We Offer
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1
Protocol Writing
Our experts develop clear, compliant, and well-structured clinical trial protocols, ensuring alignment with regulatory guidelines and study objectives. We create detailed documents covering study design, endpoints, eligibility criteria, and data collection methods, optimizing trial efficiency and compliance.
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2
Manuscript Writing
We specialize in crafting high-quality, publication-ready manuscripts that effectively communicate clinical trial findings. Our expert medical writers ensure clarity, accuracy, and compliance with journal guidelines, enhancing the impact of research.
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3
Clinical Study Reports
Our expert medical writers collaborate with medical teams and statisticians to develop comprehensive, accurate, and regulatory-compliant Clinical Study Reports (CSRs). We ensure clarity, adherence to ICH E3 guidelines, and alignment with sponsor-specific requirements.
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4
Publications
We provide end-to-end publication support, ensuring clinical research findings are effectively communicated in peer-reviewed journals, conference proceedings, and scientific forums. Our expert medical writers craft clear, accurate, and impactful manuscripts, abstracts, and posters while adhering to journal and regulatory guidelines.
