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[Changes in the German Medicinal Product Act imposed by the EU regulation on clinical trials]

Lars Nickel1, Yvonne Seibel1,2, Marion Frech3

  • 1Bundesministerium für Gesundheit, Bonn, Deutschland.

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|July 1, 2017
PubMed

Keywords:
Clinical TrialsEuropean Clinical Trials RegulationFourth Law amending the Medicinal Products ActMedicinal Products Act

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