subject: Medical Equipment Suppliers Uk [print this page] The medical supply and production in the Europe are much different from the Asia. In the Europe they have the European legal frame work [EU]. It aims to remove technical barriers to trade and dispel the consequent uncertainty for economic operators allowing for the free movement of goods inside the EU.
The core legal framework consists of 3 directives:
* Directive 90/385/EEC regarding active implantable medical devices;
* Directive 93/42/EEC regarding medical devices;
* Directive 98/79/EC regarding in vitro diagnostic medical devices.
They aim at ensuring a high level of protection of human health and safety and the good functioning of the Single Market. These 3 main directives have been supplemented over time by several modifying and implementing directives, including the last technical revision brought about by Directive.
In UK the Medicines and Healthcare products Regulatory Agency (MHRA) acts as a CA.
The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK government agency which is responsible for ensuring that medicines and medical devices work and are acceptably safe.
The agency was formed on 1 April 2003 with the merger of the Medicines Control Agency (MCA) and the Medical Devices Agency (MDA). It is an executive agency of the Department of Health.
The Basic Roles of the MHRA
1. Operate post-marketing surveillance for reporting, investigating and monitoring of adverse drug reactions to medicines and incidents with medical devices.
2. Assessment and authorization of medicinal products for sale and supply in UK.
3. Oversee the Notified Bodies that ensure medical device manufacturers comply with regulatory requirements before putting devices on the market.
4. Operate a quality surveillance system to sample and test medicines to address quality defects and to monitor the safety and quality of unlicensed products.
5. Investigate internet sales and potential counterfeiting of medicines, and prosecute where necessary.
6. Regulate clinical trials of medicines and medical devices.
7. Monitor and ensure compliance with statutory obligations relating to medicines and medical devices.
8. Promote safe use of medicines and devices.
9. Manage the General Practice Research Database and the British Pharmacopoeia.
MHRA hosts and supports a number of expert advisory bodies, including the Commission on Human Medicine which replaced the Committee on the Safety of Medicines in 2005, and the British Pharmacopoeia Commission.
As part of the European system of approval, MHRA or other national bodies can be the rapporteur or co-rapporteur for any given pharmaceutical application, taking on the bulk of the verification work on behalf of all members, while the documents are still sent to other members as and where requested.
