Medical writing
Neuvantics offers a comprehensive suite of medical writing services delivered by our experienced Medical Writers who are well-versed in ICH E3 guidelines. Our team works closely with key operational departments to gather and integrate vital information, ensuring a deep understanding of your research objectives. With extensive therapeutic expertise, our writers are adept at creating high-quality documents tailored to your specific needs, while maintaining the highest standards of accuracy and clarity.
Our medical writing services include the preparation of clinical trial reports, study protocols, informed consent forms, regulatory submissions, and other critical documents. Neuvantics ensures that all deliverables are in full compliance with relevant regulatory requirements and ICH guidelines. By maintaining close communication with sponsors, we ensure that study findings are presented clearly and concisely, meeting both scientific and regulatory expectations. Whether you require documents for regulatory authorities or internal use, Neuvantics’ medical writers provide professional and precise content to support the success of your clinical trials.
Our Medical writing services include:
- Development of study protocols, amendments, and administrative updates
- Creation of Informed Consent Forms (ICFs)
- Narratives for Serious Adverse Events (SAE)
- Preparation of annual safety documentation
- Compilation of Clinical Study Reports (CSRs)
- Creation of Integrated Summary of Safety (ISS) reports
- Generation of Integrated Summary of Efficacy (ISE) reports
- Drafting of Standard Operating Procedures (SOPs)