Integrating critical skill sets into your development process.
The quality and level of involvement of Medical Writers during the drug development life cycle can have a significant impact on the time-to-market for your products. When Medical Writers are brought in at the beginning of a development program or study, they can streamline the process by helping the team to plan for the study report.
With decades of experience providing services for some of the world’s largest pharmaceutical and biotechnology companies, as well as small- to mid-size Life Sciences companies, our highly-skilled Medical Writers are dedicated to taking the worry and frustration out of the medical writing process. Our team can help you manage peak workloads, or we can act as your outsourced team to handle your Medical Writing needs on an ongoing basis. Comprehensive Medical Writing services include:
- Clinical Study Reports (CSRs)
- Protocols and Amendments
- Investigational New Drug Applications (INDs)
- Data Safety Monitoring Board (DSMB) reports
- Clinical Trial Annual Reports
- Summary Documents
- Investigator Brochures
- Safety Updates
- Safety Narratives
- Abstracts and Publications
- Post-Marketing Publications including Abstracts, Case Studies, Patient Information Pamphlets and Presentations Targeted to MDs and Formularies
Experis Clinical Development Practice Medical Writers are members of the American Medical Writers Association and frequently participate at AMWA and Drug Information Association annual conferences and meetings.