Valsts valodas centra izstrādātie medicīnas zinātņu, farmācijas un veterinārmedicīnas termini

Konteksts: [..] In addition to the provisions laid down in paragraph 1, where an application is made for a new indication for a well-established substance, a non-cumulative periodof one year of data exclusivity shall be granted, provided that significant pre-clinical or clinical studies were carried out in relation to the new indication [..]
Avots: Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use