|Welcome to the website of Metaxon
your service provider for clinical trial documentation
Our services include but are not limited to:
- compilation of Trial Master Files, Investigatior Site Files, submission dossiers and other study related binders
- screening of Trial Master Files, case report forms and other documents for completeness, accuracy and possible discrepancies
- reconciliation of hard copy documents and electronic files
- drafting of file notes
- translations of all clinical study related documents from German, English, French, Spanish, Hungarian or Romanian into German or English (other languages upon request)
We perform all our assignments according to the Guideline for Good Clinical Practice as per the International Conference of Harmonisation of technical requirements for registration of pharmaceuticals for human use (E6(R1), June 1996) and in compliance with the the Declaration of Helsinki - ethical principles for medical research involving human subjects (64th WMA General Assembly, Brazil, October 2013), respecting country specific requirements, as well as the guidelines and Standard Operating Procedures of your company.
|For trial documentation specific enquiries, please contact:
Géza Henrik VARGA, M.Sc.
8006 Zürich, Switzerland
+41 78 695 31 13
|Regarding translations, please direct your question to:
Lilla BALAZS, Ph.D.
Chemin des Ribaudes 26
2000 Neuchâtel, Switzerland
+41 77 467 64 28