Adrem Research Communications provides a full range of medical writing services for the clinical research community.
We have extensive experience writing, editing, and reviewing Regulatory and other Scientific documents. We integrate this with our thorough understanding of the CFR, ICH Guidelines, and GCP to provide each of our clients with expert and efficient medical writers. In addition, we offer professional document preparation and formatting (including Microsoft Word, Excel, and Power Point).
Regulatory and Other Scientific Documents
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The following is a list of the most common documents for which we provide services:
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- Clinical Study Reports
- Protocols
- Investigator Brochures
- CTDs/NDAs
- Periodic Safety Reports
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- Subject Narratives
- Synopses
- Informed Consent Forms
- Abstracts
- Manuscripts
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Indications
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Our staff has experience in a variety of indications, including, but not limited to:
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- Cancer
- Inflammatory Diseases
- Central Nervous System Disorders
- Diabetes
- Lipid-Controlling Agents
- Hepatitis C Virus
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