Back to Results
First PageMeta Content
Pharmaceuticals policy / Health care / Health / Pharmaceutical industry / Medical research / Healthcare quality / European Medicines Agency / European Union / Qualified Person Responsible For Pharmacovigilance / Marketing authorization / Summary of Product Characteristics / Pharmacovigilance


B.08 GUIMA Transfer national requirements AT BE CZ DE(BVL, PEI) EE ES FI FR IE IS IT LT LV NL PL RO SE SK SI UKEMA-CMDv
Add to Reading List

Document Date: 2016-02-02 09:57:36


Open Document

File Size: 225,29 KB

Share Result on Facebook