Submission: {{data.metadata.regActivity}}

Product Type:

Submission format:

Sequence number:

Related sequence:

Clinical data for publication - Final Version:

Complete
Partial

Confirmation that the clinical reports submitted for scientific evaluation are the same as those submitted for publication, in the Redaction proposal and Final Redacted Versions, except for the redactions:

RMP included:

Brexit related procedure:

RMP version Number

Select Pam Code:

Select a Product:

{{shortProduct.shortName}} Sequence number: {{shortProduct.sequenceNumber}}

MAH name	PO number
{{sn}}

Product EMA number:

Product short name:

ATC Code:

INN:

MAH:

Please provide the name(s) of any centrally authorised medicinal product for which the same change(s) are being applied for outside of this procedure:

Is this ancillary device:

Select a Procedure Number:

Grouping (more than one scope):

Add Related Procedure

Grouping (more than one scope):

Select WS/IG number:

Renewal type:

1 year conditional
5 year

Customer number

Customer reference

Sequence number must be 4 digit number.
Please confirm that the clinical reports submitted for scientific evaluation are the same as those submitted for publication.
Please select Clinical d/f publication - Final Ver
Please select pam code
Please provide MAH name
No products have been selected.
No national products have been selected.
No grouping or worksharing numbers have been selected.
Select at least one presentation for product {{data.errors.presentationNotSelectedProductName}}.
Please provide customer number
Please provide customer reference
Please provide valid related sequence number
Duplicate application number is selected
Sequence number must be greater than related sequence number