The medical writers at LINK are highly qualified in life sciences and have writing experience from a wide range of therapeutic areas.
Our medical writers form a part of the Biometrics Department and work in close cooperation with statisticians, data managers and personnel qualified in regulatory affairs in order to ensure that all documents meets the required submission standards.
Our services include writing of documents for regulatory/pharmaceutical purposes, and for medical communication:
- Clinical study reports (Phases I-IV)
- Clinical study protocols
- Investigators brochures
- Patient narratives/Safety reports
- Manuscripts for publication in peer-reviewed scientific journals
- Literature reviews
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