Valsts valodas centra izstrādātie medicīnas zinātņu, farmācijas un veterinārmedicīnas termini

Konteksts: [..] Competent Authorities should ensure that Healthcare Professionals, Patients/Consumers and the general public are informed, where appropriate, of any significant changes in the Product Information (Summary of Product Characteristics and Package Leaflet) and of any suspected safety concerns requiring vigilance [..]
Avots: VOLUME 9A of The Rules Governing Medicinal Products in the European Union - Guidelines on Pharmacovigilance for Medicinal Products for Human Use -