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Services
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Medical Writing Peachtree’s medical writers are part of an interdisciplinary reporting team that provides support to our clients at all stages of the drug development process. Peachtree’s writers work on clinical study reports, patient narratives, regulatory submissions, manuscripts, protocols, newsletters, posters, investigator brochures, annual safety reports and periodic safety update reports. Regulatory submission deliverables include: integrated summaries of safety and efficacy, clinical sections of the Common Technical Document and electronic publishing. The medical writing group at Peachtree possesses both significant scientific strength and substantial international writing and regulatory experience. The Peachtree medical writing team possesses extensive experience in the pharmaceutical industry. Peachtree's medical writers have access to standard templates that meet regulatory standards and are also practiced in using report templates that may be provided by our clients. Peachtree's writers have a variety of software available, so that they can provide the report to the client in whatever electronic or hard copy format may be needed. At each stage of the writing process, our clients review and modify the study report so that it fully meets the needs of their development program. In addition, at each stage the report undergoes a rigorous quality control process, which employs team review, peer review and final QC.
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