Med Communications now offers Regulatory Writing services
Med Communications’ newest service area, Regulatory Writing, offers support across all stages of clinical drug development:
- Clinical Trial Protocol Development
- Investigator’s Brochures
- Clinical Study Reports
- Submission Support
- Quality Control
- Safety Narratives
- Aggregate Safety Reports
- Clinical Trial Publications
Our scientist-writers collaborate seamlessly with your organization to craft content tailored to your regulatory requirements and timelines. We offer flexible engagement models, including functional service provider arrangements, hourly rates, and project-level contracts, to best meet your company’s needs.
With extensive expertise across various regulatory documents and therapeutic areas, we have a deep understanding of the regulatory approach to document review and how it integrates with lean authoring principles. Our team is equipped to guide your organization in producing concise and compliant regulatory documents. Additionally, we provide “rescue regulatory writing” services if your current partner falls short of the quality and service levels you require.
We recognize that content is just one aspect of achieving success. Our regulatory writers possess the organizational, communication, and collaborative skills necessary to manage your project from inception to completion. Our comprehensive services include timeline development, individual document management, and submission management to ensure all your regulatory needs are met effectively.
Visit our Regulatory Writing page to learn more about the services we offer, then contact us today to explore how we can support your regulatory writing needs: 877-477-0977 or https://medcommunications.com/contact-us/.
