Back to Results
First PageMeta Content
Research / Health / Pharmacology / European Union / Pharmaceutical industry / European Medicines Agency / Supplementary protection certificate / Qualified Person Responsible For Pharmacovigilance / Clinical Trials Directive / Pharmaceuticals policy / Clinical research / Pharmaceutical sciences


L[removed]EN Official Journal of the European Union
Add to Reading List

Document Date: 2013-10-09 08:52:52


Open Document

File Size: 179,57 KB

Share Result on Facebook

Company

Agency for the Evaluation / /

Event

Product Issues / /

IndustryTerm

pharmaceutical form / generic medicinal products / generic medicinal product / reference medicinal product / authorised medicinal products / treatment of acquired immune deficiency syndrome / pharmaceutical and pre-clinical tests / manufacturing process characteristics / pharmaceutical industry / treatment of auto-immune diseases / immediate-release oral pharmaceutical forms / orphan medicinal product / reference product / biological medicinal product / defective products / homeopathic medicinal products / readyto-use pharmaceutical / to medicinal products / manufacturing practice / pharmaceutical / pharmaceutical particulars / medicinal products / food supplements / manufacturing processes / food / homeopathic manufacturing procedure / radiopharmaceutical products / given product / certain medicinal products / chemical description / pharmaceutical forms / chemical name / subsequent applications / law relating / medicinal product / waste products / regulated products / patent law / unauthorised medicinal product / pharmaceutical legislation / chemical / immunological medicinal products / chemical agents / homeopathic medicinal product / coordination / orphan medicinal products / reference biological product / /

MedicalCondition

auto-immune diseases / acquired immune deficiency syndrome / viral diseases / neurodegenerative disorder / cancer / disease / diabetes / /

MedicalTreatment

radiation / gene therapy / /

Organization

World Health Organization / European Economic and Social Committee / EUROPEAN PARLIAMENT / COUNCIL OF THE EUROPEAN UNION / European Agency for the Evaluation of Medicinal Products / Committee of the Regions / European Union / Official Medicines Control Laboratory / /

Position

Official / forward data demonstrating / Representative of the marketing / representative / EN Official / local representative / /

Product

products / /

ProgrammingLanguage

EC / L / /

PublishedMedium

the Official Journal / /

Technology

radiation / information technologies / radiopharmaceuticals / gene therapy / /

SocialTag