Medical Writing Services
At ScientificWrite, we specialize in delivering high-quality, regulatory-compliant, and scientifically accurate medical writing services.
Our mission is to support pharmaceutical companies, biotech firms, CROs, and academic researchers by transforming complex medical data into clear, concise, and impactful documents.
With a strong foundation in clinical research, regulatory requirements, and scientific communication, we ensure that every document we create aligns with global standards and reflects your organization's credibility and excellence.
Our Medical Writing Solutions Include:
Preparation of clinical study protocols, investigator brochures, clinical study reports (CSRs), informed consent forms (ICFs), and regulatory submission dossiers (IND, NDA, BLA, MAA).
Authoring of essential documents for clinical development phases — including study designs, patient narratives, and safety reports (DSURs, PSURs).
- Regulatory Medical Writing
- Clinical Trial Documents
- Publication Writing
- Medical Communications
- Health Economics and Outcomes Research (HEOR)