Valsts valodas centra izstrādātie ķīmijas un ķīmiskās tehnoloģijas termini

Konteksts: [..] Revision of introduction to comply with Directive 2001/83/EC and Directive 2001/82/EC, as amended by Directives 2004/27/EC and 2004/28/EC, respectively, following consultation of the public, the Ad Hoc Working Group of GMP Inspectors, the Pharmaceutical and the Veterinary Pharmaceutical Committee [..]
Avots: EudraLex. The Rules Governing Medicinal Products in the European Union. Volume 4. EU Guidelines to Good Manufacturing Practice. Medicinal Products for Human and Veterinary Use. Part II Basic Requirements for Active Substances used as Starting Materials.