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Writing and revising of regulatory documents

  • CTD non-clinical modules (2.4, 2.6, 4)
     
  • CTD clinical modules (2.5, 2.7, 5)
     
  • clinical study reports to ICH standards
     
  • investigator brochures



Writing and revising
of medical and scientific communications


Other services

  • supervision and support for all stages of scientific document writing
     
  • review and quality assurance of existing data for regulatory purposes
    or publication
Pyramide

Dr. rer. nat. Petra A. Schwantes   I   +49 (0) 9505 6775   I    info@biomedicalservices.de