<--- Back to Details
First PageDocument Content
European Union directives / Clinical research / Directive 93/41/EEC / Pharmaceuticals policy / Toxicology / ISIRI 13146 / Evaluation / Reference / Standards
Date: 2014-07-29 14:28:15
European Union directives
Clinical research
Directive 93/41/EEC
Pharmaceuticals policy
Toxicology
ISIRI 13146
Evaluation
Reference
Standards

Add to Reading List

Source URL: www.agriculture.gov.ie

Download Document from Source Website

File Size: 15,51 KB

Share Document on Facebook

Similar Documents

Fisheries law / Pharmaceuticals policy / Common Fisheries Policy / Economy of the European Union / Fisheries management / Illegal / unreported and unregulated fishing / Fishery / Directive 93/41/EEC / Directive 75/318/EEC

AACL BIOFLUX Aquaculture, Aquarium, Conservation & Legislation International Journal of the Bioflux Society Latest legislation issues on sustainable exploitation of aquatic resources

DocID: 1p3Ql - View Document

Health / Technology / Clinical research / Food safety / Product safety / Prevention / Directive 93/41/EEC / Good Laboratory Practice / Pharmaceuticals policy / Packaging / European Union directives

NATIONAL PROGRAMME Chapter 6 Agriculture

DocID: 1gqFg - View Document

Health / Medicine / European Union / Good Laboratory Practice / Directive 93/41/EEC / Pharmaceuticals policy / European Union directives / Clinical research

2004R0882 — EN — — — 1 This document is meant purely as a documentation tool and the institutions do not assume any liability for its contents ►B REGULATION (EC) NoOF THE EUROPEAN

DocID: 1aIQk - View Document

Law / European Union / Directive 93/41/EEC / Council Implementing Regulation (EU) No 282/2011 / Pharmaceuticals policy / Clinical research / European Union directives

STATUTORY INSTRUMENTS S.I. No. 566 of 2008 ————————

DocID: 183gu - View Document

Public administration / European Aviation Safety Agency / Rulemaking / Government / Directive 93/41/EEC / Joint Aviation Authorities / United States administrative law / Transport / Pharmaceuticals policy

CS-25 Amendment 10 Explanatory Note European Aviation Safety Agency Rulemaking Directorate

DocID: 16lap - View Document