In order to facilitate the exchange of information on pharmacovigilance within the Community, the Commission, after consulting the Agency, the Member States and interested parties, shall draw up guidelines on the collection, verification and presentation of adverse reaction reports, including technical requirements for electronic exchange of pharmacovigilance information in accordance with internationally agreed formats, and shall publish a reference to an internationally agreed medical terminology.
Za lažjo izmenjavo informacij o farmakovigilanci v Skupnosti, Komisija, po posvetovanju z Agencijo, državami članicami in zainteresiranimi strankami, izdela navodila za zbiranje, preverjanje in predstavitev poročil o neželenih učinkih, vključno s tehničnimi zahtevami za elektronsko izmenjavo podatkov o farmakovigilanci v skladu z mednarodno dogovorjenimi oblikami ter objavi napotilo na mednarodno sprejeto medicinsko terminologijo.