To provide industry-leading expertise, progressive strategy, consistent performance, and services customised specifically to the needs of each of clients and customers.
- Non Clinical Documentation
- Clinical Documentation
- Medical Affairs
- Regulatory Documentation
- Medico Marketing
- Non-Clinical Documentation: CTD Module 2.4, Module 2.6 and Module 4
- Clinical Documentation: CTD Module 2.5, Module 2.7, Module 5, Clinical Trial Protocols – Phase I to IV, Investigator’s Brochures and Updates, Clinical Study Reports: Synopsis, Abbreviated, Interim, and Final, Narratives
- Medical Affairs: Manuscripts, Abstracts, Posters, Research/Review articles, Post meeting reports, Slide decks
- Regulatory Documentation: Authoring / Updating of New / Existing Company Core Data Sheets (CCDS), Responding to Health Authority Queries, Biowaiver Reports, Bibliographic Summaries, Bridging BE Reports
- Medico Marketing: Educational material for patients, Healthcare professionals and Pharmaceutical industry personnel, Product website content (for both scientific and patient audiences)
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