Application Files ("dossiers")

  • preparation and submission of all application files (dossiers) for Europe (EMEA, MRP, national applications) and/or Switzerland (Swissmedic, BAG and BSV) (new products,re-registrations, etc.)
  • support for the entire registration strategy on the basis of regulatory aspects
  • constructive analysis and completion of existing documentation (for group revisions or a re-registration attempt)
  • reply to inquiries from the authorities (re-registration attempts)