Medical Writing Services
Documenting your clinical trials in the most effective way is critical to getting your product to market. We can help you write a wide array of documents to support your clinical research at any point in development, including.
Documenting your clinical trials in the most effective way is critical to getting your product to market. We can help you write a wide array of documents to support your clinical research at any point in development, including:
- Product development plans
- Investigator brochures
- Literature reviews
- Trial protocols and amendments
- Model informed consent forms
- DSMB reports
- Patient narratives
- Clinical study reports
- Manuscripts
- Regulatory submissions in electronic or paper formats
All our medical writing services are compatible with ICH guidelines and other regulatory requirements. Along with our high level of internal quality control for our writing projects, we can tap into Quintiles’ extensive network of medical, scientific and technical professionals for additional input, reviews and implementation.
With complementary Quintiles expertise in pharmacokinetics and pharmacodynamics, commercial medical communications, pharmacovigilance and regulatory affairs including our well-established Regulatory Document Publishing group, Quintiles is truly a one-stop shop for all your documentation needs.