Blank Report Template - European Medicines Agency - Europa

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28 Οκτ 2013 (πριν από 3 χρόνια και 5 μήνες)

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7 Westferry Circus


Canary Wharf


London E14 4HB


United Kingdom

An agency of the European Union



Telephone

+44 (0)20 7418 8400

Facsimile

+44 (0)20
7418 8416

E
-
mail

info@ema.europa.eu

Website

www.ema.europa.eu





12

June

2012

EMA/358526/2012


Patient Health Protection


EMA
/EC

websit
e references

substituting information previously available in Notice to
Applicants


Chapter 7 of Volume 2A



NtA, Chapter 7 (Volume 2A)

Section heading

Name of the updated

EMA/EC
document

EMA/EC website references

location


1.

FORMAT FOR
APPLICATION IN THE EU

The Rules Governing Medicinal Products in the
European Union, Vol. 2B and Vol. 2C


Dossier Submission: Regulatory and procedural
guidance



Dossier Format: Regulatory and procedural
guidance

http://ec.europa.eu/health/documents/eudralex/
vol
-
2/index_en.htm


http://
www.ema.europa.eu/ema/index.jsp?curl=
pages/regulation/document_listing/document_lis
ting_000121.jsp&mid=WC0b01ac0580027255


http://www.ema.europa.eu/ema/index.jsp?curl=
pages/regulation/document_listing/document_lis
ting_000102.jsp&mid=WC0
b01ac058002c599


2.

LANGUAGES TO BE USED FOR DOSSIER,
EMA pre
-
authorisation procedural advice for users
http://www.ema.europa.eu/ema/index.jsp?curl=


EMA/EC website references substituting information previously available in Notice to Applicants


Chapter 7 of Volume 2A






Page
2
/
5



NtA, Chapter 7 (Volume 2A)

Section heading

Name of the updated

EMA/EC
document

EMA/EC website references

location


RESPONSES, VARIATIONS AND
RENEWALS

of the centralised procedure

-

Question 23


pages/regulation/general/general_content_0001
57.jsp&mid=WC0b01ac058002251f

European Medicines Agency post
-
authorisation
procedural

advice for users of the centralised
procedure

Type IA Variations


Q1.11

Type IB Variations


Q2.9

Type II Variations


Q3.11

Type II Variations/Ext. app

Q4.10

Worksharing of variations


Q6.10

Annual Re
-
assessment


Q8.11

Renewal


Q9.11

Art 61(3)
Notifications


Q15.9


http://www.ema.europa.eu/ema/index.jsp?curl=pages/
regulation/general/general_content_000166.jsp&mid=
WC0b01ac0580023399


3.

NUMBER OF COPIES OF THE DOSSIER,
RESPONSES, VARIATIONS AND
RENEWALS

EMA pre
-
authorisation procedura
l advice for users
of the centralised procedure


-

Question 23


http://www.ema.europa.eu/ema/index.jsp?curl=
pages/regulation/general/general_content_0001
57.jsp&mid=WC0b01ac058002251f


European Medicines Agency post
-
authorisation
procedural

advice for users of the centralised procedure


Type IA Variations


Q1.4

Type

IB Variations


Q2.4

Type II Variations


Q3.4

Type II Variations/Extension app.


Q4.4

Grouping of Variations


Q5.3

Worksharing of variations


Q6.4

Changing the Name


Q7.3


ht t p://www.ema.europa.eu/ema/index.jsp?curl=pages/
regulat ion/general/general_content_000166.jsp&mid=
WC0b01ac0580023399




EMA/EC website references substituting information previously available in Notice to Applicants


Chapter 7 of Volume 2A






Page
3
/
5



NtA, Chapter 7 (Volume 2A)

Section heading

Name of the updated

EMA/EC
document

EMA/EC website references

location


Annual Re
-
assessment


Q8.3

Renewal


Q9.3

FUMs & SOs


Q10.4

PSURs


Q11.9

Art

46


Q12.3

Transfer of MA


Q13.2

Art 61(3) Notifications


Q15.4

Marketing & Cessation notification

-

Q16.6

4.

DOSSIER
CHECK
-
IN PROCEDURE

EMA pre
-
authorisation procedural advice for users
of the centralised procedure


-

Question 23

http://w
ww.ema.europa.eu/ema/index.jsp?curl=
pages/regulation/general/general_content_0001
57.jsp&mid=WC0b01ac058002251f

5.

MOCK
-
UPS, SPECIMENS AND SAMPLES

EMA pre
-
authorisation procedural advice for users
of the centralised procedure

-

Question 14

http://www.ema.europa.eu/ema/index.jsp?curl=
pages/regulation/general/general_content_0001
57.jsp&mid=WC0b01ac058002251f


European Medicines Agency post
-
authorisation
procedural

advice for users of the centralised
procedure


Type IA Variations


Q1.9

Type IB Variations


Q2.8

Type II Variations


Q3.10

Type II Variations/Extension app.


Q4.9

Changing the Name

Q7.4

Annual Re
-
assessment

Q8.10

Renewal

Q9.10

Transfer of MA Q13.9

Art 61(3) Notifications Q15.8

ht t p://www.ema.europa.eu/ema/index.jsp?curl=pages/
regulat ion/general/general_content_000166.jsp&mid=
WC0b01ac0580023399




EMA/EC website references substituting information previously available in Notice to Applicants


Chapter 7 of Volume 2A






Page
4
/
5



NtA, Chapter 7 (Volume 2A)

Section heading

Name of the updated

EMA/EC
document

EMA/EC website references

location



6.

NATIONAL PROCEDURE AFTER A
COMMISSION DECISION ON A REFFERAL

N/A

N/A

7.

LIST OF OFFICIAL JOURNALS

N/A

N/A

8.

ADDRESSES FOR DELIVERY OF THE
DOSSIER AND SUBSEQUENT
CORRESPONDENCE

EMA pre
-
authorisation procedural advice for users
of the centralised procedure

-

Question 23

http://www.ema.europa.eu/ema/index.jsp?curl=
pages/regulation/general/general_content_0001
57.jsp&mid=WC0b01ac0
58002251f

European Medicines Agency post
-
authorisation
procedural

advice for users of the centralised
procedure


Type IA Variations


Q1.4

Type IB Variations
-
Q2.4

Type II Variations


Q3.4

Type II Variations/Extension app.


Q4.6

Worksharing of
variations


Q6.5

Annual Re
-
assessment


Q8.4

Renewal


Q9.5

FUMs & SOs

Q10.5

PSURs


Q11.12

Art 46

Q12.4

Transfer of MA


Q13.3

Art 61(3) Notifications


Q15.5

Marketing & Cessation notification


Q16.4, Q16.5

ht t p://www.ema.europa.eu/ema/index.jsp?curl
=pages/
regulat ion/general/general_content_000166.jsp&mid=
WC0b01ac0580023399


9.

ADDRESSES FOR RECEIPT OF FEES AND
TERMS OF PAYMENT

EMA pre
-
authorisation procedural advice for users
of the centralised procedure

-

Questions 10, 11, 12, 13


http://www.ema.europa.eu/ema/index.jsp?curl=
pages/regulation/general/general_content_0001
57.jsp&mid=WC0b01ac058002251f

E
uropean Medicines Agency post
-
authorisation
procedural

advice for users of the centralised
procedure

ht t p://www.ema.europa.eu/ema/index.jsp?curl=pages/
regulat ion/general/general_content_000166.
jsp&mid=


EMA/EC website references substituting information previously available in Notice to Applicants


Chapter 7 of Volume 2A






Page
5
/
5



NtA, Chapter 7 (Volume 2A)

Section heading

Name of the updated

EMA/EC
document

EMA/EC website references

location



Type IA Variations


Q1.8

Type IB Variations

Q2.7

Type II Variations


Q3.9

Type II Variations/Extension app.


Q4.8

Grouping of Variations

Q5.8

Worksharing of variations


Q6.9

Annual Re
-
assessment


Q8.8

Renewal


Q9.7

FUMs & SOs

Q10.8

Art 46


Q12.6

Transfer of MA


Q13.6

Art 61(3) Notifications


Q15.7

WC0b01ac0580023399


10.

‘BLUE
-
BOX’ REQUIREMENTS

EMA pre
-
authorisation procedural advice for users
of the centralised procedure


-

Question 14

-

Question 6

http://www.ema.europa.eu/ema/index.jsp?curl=
pages/regulation/general/general_content_0001
57.jsp&mid=WC0b01ac058002251f




GUIDELINE ON THE PACKAGING

INFORMATION OF MEDICINAL PRODUCTS

FOR HUMAN USE AUTHORISED BY THE

COMMUNITY

http://ec.europa.eu/health/documents/eudralex/vol
-
2/index_en.htm