ProPharma Group’s writers, editors, and quality reviewers know what it takes to produce clear, concise text for your clinical, scientific, and regulatory needs.
ProPharma Group: Your Expert Medical Writing Partner
Regardless of where you are in the development of your product, our team of medical writers has the expertise you need. Some of our medical writing-related services include:
Clinical and Nonclinical
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- Biologics License Applications (BLAs)
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- Clinical Study Reports (CSRs) and narratives
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- Transparency and Clinical Trial Disclosures (CTDs) and posting
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- Drug Safety Update Reports (DSURs) and Periodic Safety Update Reports (PSURs)
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- General investigational plans
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- Investigator Brochure (IB) submissions
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- Medical device Clinical Evaluation Reports (CERs)
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- Pediatric Indication Plans (PIPs)
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Project Support
- Compilation, hyperlinking, and publishing
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- Word processing and formatting
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- Style-guide and template creation
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- Content editing & proofreading, including a QC review of data against the text and source documents
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- Literature searches, analysis, reference libraries, and citations
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- Standard operating procedure (SOP) development
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- Populating tables and building figures
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Publications
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- Continuing Medical Education (CME) program planning
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