Quality Review of Documents Product Information Templates

Identifier 200000029859
Term Name
Obligation to conduct post-authorisation measures
- Translation Status CURRENT
- Modified on 2024-08-27

Status CURRENT
Domain Human use - H
Parent
- D. CONDITIONS OR RESTRICTIONS WITH REGARD TO THE SAFE AND EFFECTIVE USE OF THE MEDICINAL PRODUCT
Hierarchy
- Obligation to conduct post-authorisation measures (level=H3) / D. CONDITIONS OR RESTRICTIONS WITH REGARD TO THE SAFE AND EFFECTIVE USE OF THE MEDICINAL PRODUCT (level=H2) / ANNEX II (level=H1)
Data Classification PUBLIC
Extended Attributes
- Is blank subsection allowed N
- Is Mandatory N
- Product Information Document Type Annex II
- Regulatory Authorisation/Registration Procedure Centralised Procedure - CP
- Sequence Order 69