Standing Committee on "Veterinary Medicinal Products",, Brussels - Main contents
date | June 4, 2019 |
---|---|
city | Brussels, Belgium |
organisation | Standing Committee on veterinary medicinal products (C02900) i |
CMTD(2019)0583 (Committee meeting)
DG Health and Food Safety
Title:
Standing Committee on "Veterinary Medicinal Products", 4 June 2019
Date:
04 Jun 2019
Committee:
Standing Committee on veterinary medicinal products
Associated Documents:
S062904/01 (Summary record)
Title:
Summary record - meeting of 4 June 2019 of the Standing Committee on Veterinary Medicinal Products
V062671/01 (Voting sheet)
Title:
Formal results of voting on Commission Implementing Decision granting marketing authorisation under Regulation (EC) No 726/2004 of the European Parliament and of the Council for "HorStem - equine umbilical cord mesenchymal stem cells", a veterinary medicinal product.
A062217/01 (Agenda)
Title:
Agenda for meeting of 4 June 2019 of the Standing Committee on Veterinary Medicinal Products.
D061630/03 (Draft implementing measure/act)
Title:
COMMISSION IMPLEMENTING DECISION granting marketing authorisation under Regulation (EC) No 726/2004 of the European Parliament and of the Council for "HorStem - equine umbilical cord mesenchymal stem cells", a veterinary medicinal product
D061630/02 (Draft implementing measure/act)
Title:
Draft COMMISSION IMPLEMENTING DECISION of XXX granting marketing authorisation under Regulation (EC) No 726/2004 of the European Parliament and of the Council for "HorStem - equine umbilical cord mesenchymal stem cells", a veterinary medicinal product
Contents
Basic legal act(s):
Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance) Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance ) Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products Council Regulation (EEC) No 2377/90 of 26 June 1990 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin