Mhra License Ensures All Medicines and Medicinal Products Sold or Exported From the UK are Safe

UK pharmacies that are manufacturing and exporting pharmaceutical products and solutions need to possess Mhra license. MHRA is a government body that is responsible for regulating all medicines and medical devices in the UK by ensuring they are safe to use. The main goal of MHRA is to safeguard public health through a system of regulation. 

Pharmaceutical manufacturers and distributors in the UK need to apply for the Mhra license which is given only after the body conducts an inspection and finds the manufacturers and distributors conforming to internationally agreed standards. Also, the medicines should be manufactured, stored and distributed in compliance with the required regulatory standards.

A pharmacy is not allowed to sell or market medical products in the UK without securing the necessary license. The companies that are involved in all stages of the manufacture and distribution of pharmaceutical products need to have the relevant licence for the activity. MHRA works in accordance with the Human Medicines Regulations 2012 in regulating the UK medicine market.

You can also apply for Mhra license if you are into the business of exporting medicines and medicinal products. The MHRA issues export certificates as applied by the UK pharmacies to help exporters of medicinal products satisfy the import requirements of other countries. MHRA certificate will ensure the exported products meet all the statutory requirements. In some cases, the certificates are formatted to comply with international organisations such as the World Health Organisation (WHO). 

Guidance provided by MHRA and other government organisations ensure every UK manufacturer and distributor of medicines and medicinal devices meet their obligations to reduce chances of affecting the health of human beings who will buy their products.