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Study Protocol development |
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Designing Case Report Forms |
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Developing Informed Consent Form (ICF) |
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Compilation of Investigator's Brochure (IB) |
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SOP writing |
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Documentation for Regulatory Submission |
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ICH E3 compliant CSRs (Clinical Study Reports) for regulatory submission (local and global) |
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Preparing PSURs (Periodic Safety Update Reports) and ASRs (Annual Safety Reports) |
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Writing Abbreviated Reports |
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Narrative Writing |
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Manuscript Writing |
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Medical writing for Web |
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Designing letters to editors for medical journals |
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Abstracts and Poster Preparation |
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Preparing CTRD (Clinical Trial Registry Database) summaries |
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Medical and scientific literature support and reviews |
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Marketing & PR Medical Writing |
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e-learning web portals for online education |
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Training of FSO, product managers/managers |
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Drug monographs |
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Training manuals |
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Visual aids |
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Leave behind literature |
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Referencing |