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1:
H
ome
(ALT-H)
2:
H
M
A Joint
(ALT-M)
3:
H
u
man Medicines
(ALT-U)
3.1:
H
e
ads of Agencies
(ALT-E)
3.2:
C
MDh
(ALT-C)
3.3:
M
R
I Product Index
(ALT-R)
3.4:
D
i
rectory
(ALT-I)
4:
V
eterinary Medicines
(ALT-V)
You are here:
Human Medicines
>
CMDh
>
CMD subgroups / working groups
> Subgroup on Paediatric Regulation
3.2.1:
Ab
o
ut CMDh
(ALT-O)
3.2.2:
S
tatistics
(ALT-S)
3.2.3:
P
ress Releases
(ALT-P)
3.2.4:
Procedura
l
Guidance
(ALT-L)
3.2.5:
CMDh-Referrals
3.2.6:
Produc
t
Information
(ALT-T)
3.2.7:
Advice from CMDh
3.2.8:
Templates
3.2.9:
CMD sub
g
roups / working groups
(ALT-G)
3.2.9.1:
W
orking Group on Active Substance Master File Procedures
(ALT-W)
3.2.9.2:
Wor
k
ing Party on Future of the CMDh
(ALT-K)
3.2.9.3:
Subgroup o
n
Paediatric Regulation
(ALT-N)
3.2.9.4:
Subgroup on Variation Regulation
3.2.9.5:
Subgroup on Harmonisation of SmPCs
3.2.9.6:
J
oint CMDh/
PhVWP
WG
(ALT-J)
3.2.9.7:
CTS Working Group
3.2.9.8:
Joint CMDh/GCP Inspectors Subgroup
3.2.10:
Paediatric Regulation
3.2.11:
Q
uestions & Answers
(ALT-Q)
3.2.12:
Contact Form
3.2.13:
Contact Points
3.2.14:
What's new histor
y
(ALT-Y)
Subgroup on Paediatric Regulation
Mandate for the Subgroup on Paediatric Regulation
(June 2009)
Workplan 2011
Workplan 2011 on Paediatric Regulation
(January 2011)
Statistics on Paediatric Regulation
Statistics on Member States acting as rapporteurs in Paediatric worksharing procedures
(February 2011)
