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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 Harmonisation of SmPCs
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)
CMDh Subgroup on Harmonisation of SmPCs
Mandate for the CMDh Subgroup on Harmonisation of SmPCs
(November 2005)
Lists of Medicinal Products for Harmonisation of SmPCs
Final list of products for SmPC Harmonisation - 2010
(October 2010)
Criteria for selection of products for SmPC Harmonisation
(May 2011)
[
Track version]
