This includes the adaptation
of the protocol to national requirements, preparation and adaptation
of the patient information sheet and informed consent form, preparation
of the documentation required for
submission to Ethics Committees and Competent Authorities,
submission of the clinical trial
Application dossier (CTA) and regulatory follow - up.
Submission of Dossier to Foreign Country - every prospective adoptive family must submit a dossier - collection of documents that constitutes your application for adoption - to the foreign c
Dossier to Foreign Country - every prospective adoptive family must submit a
dossier - collection of documents that constitutes your application for adoption - to the foreign c
dossier - collection
of documents that constitutes your
application for adoption - to the foreign country.