
Medicines: packaging, labelling and patient information leaflets
2014年12月18日 · How to package medicines for sale and what information you must provide to consumers and healthcare professionals. The MHRA approves all packaging and labelling information for medicines sold in...
MHRA Products | Home
We publish the most up-to-date information for a medicine according to its licence history. You can use the A-Z list to find an active substance, or search for a medicine. We publish scientific...
Medicines and Healthcare products Regulatory Agency
In a UK-first, the Medicines and Healthcare products Regulatory Agency (MHRA) and Barts Health NHS Trust have developed a DNA sequencing approach that can be implemented...
The MHRA will provide a scientific opinion on new medicines that will treat, diagnose or prevent life threatening, or seriously debilitating conditions without adequate treatment options before they are formally licensed
MHRA | MHRA
Manufacturers, importers and distributors of active substances are required to register their activities with the MHRA. Since inspections of manufacturers of active substances are based on risk,...
Submitting changes to labelling and patient information leaflets
2023年12月22日 · In line with the principles of Better Regulation the MHRA has expanded the notification scheme for changes to labelling and patient information leaflets. This notification procedure provides for...
Conformity Assessment Marking - Ignitec
2023年8月8日 · Manufacturers placing products on the Great Britain market (England, Scotland, and Wales) must register their product with the Medicines and Healthcare products Regulatory Agency (MHRA) and affix a UK Conformity Assessed (UK CA) stamp on their product
GMP | MHRA
Due to the restrictions caused by COVID-19, the period of validity GMP and GDP certificates issued by MHRA is automatically extended until the end of 2024, except where clarifying remarks in the...
Medicines and Healthcare products Regulatory Agency - Wikipedia
The Medicines and Healthcare products Regulatory Agency (MHRA) is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe.
Skiny Up Derma Stamp - Titanium Derma Stamp Pen for
This item: Skiny Up Derma Stamp - Titanium Derma Stamp Pen for 【Precision Micro Needle Treatment】/ More Size for Choice/CE,ISO and MHRA Approved. (2.5mm) SAR8165