-Clinical trials: Informed Consent Forms (ICFs), protocols, case report forms, withdrawal forms.
-Submission process, including revision and updates for centralised as decentralised procedures: SPC and PIL documents, labelling material and mock-ups following EMA QRD templates and the MedDRA.
-Marketing material, questionnaires.
Quality and consistency (also with EMA terminology and phraseology) is ensured through the use of translation memories, terminology lists and my attention for detail.