Preparation of non-clinical regulatory documentation and reports

Kinesis can take care of the preparation of all non-clinical documents for regulatory submissions for various types of applications, like non-clinical reports, non-clinical overviews, summaries and tables, and contributions to Investigator’s Brochures (IBs) and IMPDs. In addition, Kinesis non-clinical experts can prepare manuscripts for scientific journals (ghostwriting) and can also help the sponsor in writing non-clinical reports when deadlines are tight and/or internal resources are not sufficient.



Consultants in drug development

Print this page