Medical Writing Services
At SPRI, we believe that each clinical document should not only be accurate — it should also present the information in a clear and straightforward manner. A poorly written document is a misunderstood document.
As clinical trials become more complex, it’s important to partner with a medical writing team that understands the current regulatory environment. SPRI maintains an experienced team of in-house medical writers, as well as a network of qualified writing partners, who have the knowledge and expertise to create a broad range of clinical documents. Make sure that your clinical documents are written clearly and accurately — let SPRI Clinical Trials match your needs with the appropriate medical writer.
Abstracts, Manuals & More
Our highly qualified medical, scientific and technical writers have in-depth knowledge in their chosen specialties, allowing them to craft well-written, data-driven documents. Whether your needs include authoring, editing, or reviewing, turn to SPRI for medical writing services.
SPRI’s technical writing capabilities include:
- Informed consents
- Protocols and amendments
- Study procedural manuals (including pharmacy manuals)
No clinical trial or topic is too complex for SPRI’s network of experienced medical writing professionals. Contact us today to learn about our medical writing capabilities. With strategic offices in the United States (New York and North Carolina), Ukraine, Russia, Georgia and Belarus and strategic partnerships in Western Europe and Australasia, we’re uniquely positioned to meet the needs of your global clinical trials.