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Medical writing

Expect no less than extensive experience from a wide range of therapeutic areas and qualifications in life sciences from our medical writers.


We ensures that all documents meet the required submission standards

As part of the Biometrics department, the medical writer will work in close cooperation with statisticians, data managers and experts in regulatory affairs. This ensures that all documents meet the required submission standards.

Our services include the writing of documents for regulatory/pharmaceutical purposes and for all other medical communication.

Services within Medical writing:

  • 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
Updated

Related contacts
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Jon B Borgaard MSc, MM
Director of Project Management 
Norway
Tel:+ 47 92 55 553
jon@linkmedical.no
280x180- Jan
Jan Hellqvist
Managing Director
Sweden 
Tel: +46 70 913 51 25
jan@linkmedical.se
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Marianne Holst
Managing Director
Denmark
Tel:+45 22 15 85 56
marianne@linkmedical.dk
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Uwe Anzenberger
Regulatory Country Manager
Germany
Tel:+49 176 8227 0156
      +49  30 2461 2025
uwe.anzenberger@linkmedical.de