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Pharmaceutical sciences / Clinical research / Executive agencies of the United Kingdom government / Department of Health / Medicines and Healthcare products Regulatory Agency / Health in the United Kingdom / Medical device / British Pharmacopoeia / Good Laboratory Practice / Medicine / Health / Pharmaceutical industry


MEDICINES AND HEALTHCARE PRODUCTS REGULATORY AGENCY FRAMEWORK DOCUMENT February 2010
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Document Date: 2011-09-23 04:48:47

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File Size: 362,22 KB

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City

York / Welwyn Garden City / Blackpool / London / /

Company

Agency for the Evaluation / /

Country

United Kingdom / Northern Ireland / /

Currency

GBP / /

Event

Product Issues / /

IndustryTerm

homoeopathic products / licensed medicinal products / blood transfusion services / hospital blood banks / higher-risk devices / healthcare products / lowest-risk devices / risk medical devices / medicinal products / /

MedicalTreatment

Herbal medicines / blood transfusion / /

Organization

Advisory Board for the Registration of Homoeopathic / European Agency for the Evaluation of Medicinal Products / Good Laboratory Practice Monitoring Authority / Government Trading Fund / Northern Ireland Assembly / MHRA / Commission for Human Medicines / Licensing Authority / STATUS Executive Agency / Executive Agency / Competent Authority for Blood Safety and Quality / Committee on the Safety of Devices / European Union / Department of Health / MEDICINES AND HEALTHCARE PRODUCTS REGULATORY AGENCY / Agency Board / /

Position

specialist advisory committees / Chairman / Minister / Northern Ireland Minister / Accounting Officer / Chief Executive 17 Senior Management Team / Minister of Health / Chairman and Chief Executive / General / head / Secretary of State / /

Product

medicines / /

ProgrammingLanguage

EC / /

Region

Northern Ireland / /

SocialTag