Framework agreement between DHSC and the Medicines and Healthcare products Regulatory Agency
In response to: Framework agreement between DHSC and the Medicines and Healthcare products Regulatory Age…
The Department of Health and Social Care and MHRA are amending the Human Medicines Regulations through draft regulations and consultation on changes to health service product information disclosure rules, aimed at benefiting NHS patients and British businesses through modernised medicines access procedures. The amendments represent significant changes to the regulatory framework governing medicines approval and provision.
In response to: Framework agreement between DHSC and the Medicines and Healthcare products Regulatory Age…
Describes the working relationship between the Department of Health and Social Care and the Medicines and Healthcare products Regulatory Agency.
The government's summary of an EU Commission proposal to amend EU legislation relating to medicinal products for human use and the impact on Northern Ireland.
The government's summary of a EU Commission proposal to amend EU legislation relating to medicinal products for human use and the impact on Northern Ireland.
The government's summary of a European Commission proposal on fees and charges payable to the European Medicines Agency.
The government's summary of an EU regulation about protein requirements for infant and follow-on formula manufactured from protein hydrolysates.