COD Research Medical writing team has extensive medical understanding, knowledge of drug development and the regulatory and safety domains. The team also has in-depth understanding of research methodologies, and awareness of relevant regulations and guidelines. with the ability to analyse, interpret, and present biomedical scientific data in the required format and good writing skills.
Our contemporary medical writing services span from the most regulated, structure-driven common technical documents such as clinical study reports (CSRs), clinical and nonclinical overviews and summaries, research documents, namely, clinical study protocols, investigational brochures (IB), or product labels such as Summary of Product Characteristics (SmPC or SPC).
Our Medical writing experts cater to a diverse range of writing across our therapeutic expertise belt. WE do not rely on the one size fits all model. It is challenging task to keep abreast of scientific, medical and regulatory happenings. However, the team has a solid foundation and has extensive expertise in:
- Protocol writing
- Scientific writing
- Report writing
- Regulatory writing
- Risk management writing
Be it battling the dynamic flow of medical misinformation in the world today or public disclosure of clinical trials, or the drifts in manoeuvring artificial intelligence and digital health, our medical writers are prudently setting trends.
Our Medical writing services are well recognized and highly sought after by our clients in the clinical development value chain.