In addition, the Plasma Master File shall provide a list of the medicinal products for which the Plasma Master File is valid, whether the medicinal products have been granted a marketing authorisation or are in the process of being granted such an authorisation, including medicinal products referred to in Article 2 of Directive 2001/20/EC of the European Parliament and of the Council relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use.
V glavni dokumentaciji o plazmi se navede seznam zdravil, za katere glavna dokumentacija o plazmi velja, če so zdravila že pridobila dovoljenje za promet ali so v postopku pridobivanja dovoljenja, vključno z zdravili, navedenimi v členu 2 Direktive 2001/20/ES Evropskega parlamenta in sveta o izvajanju dobre klinične prakse pri vodenju kliničnih preskušanj zdravil za ljudi.