Document:GBR The Human Medicines Regulations 2012 01-Jan-2025
From GxPlex
| Document information | |
|---|---|
| Reference | GBR The Human Medicines Regulations 2012 01-Jan-2025 |
| Validity area | GBR |
| Scope(s) | HM |
| Document name | The Human Medicines Regulations 2012 |
| Version / Revision | 01-Jan-2025 |
| Status | Current |
| Document type | Legal act |
| Language(s) | EN |
| Description | The Human Medicines Regulations 2012 |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
References
| Reference | Scope | Document part | Language | Preview |
|---|---|---|---|---|
| Reference:GBR The Human Medicines Regulations 2012 01-Jan-2025 Article 51B | HM | Article 51B | EN | Application for UKMA(UK) relating to generic medicinal products 51B.â(1) An applicant for a UKMA(UK) for a generic medicinal product may, by way of derogation from paragraph 10 of Schedule 8, omit ... |
