Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

European Medicines Evaluation Agency inspections

The Health Products Agency was created under Law No. 93-5 of 4 January 1993 in relation to the safety of blood transfusion products cind medicinal products (Article L 567-1 to L 567-13 of CSP). This law was intended to put in place a system of evaluation, control and inspection for medicines and make laboratories guarantee the safety of these products under the best conditions. It also envisaged the participation in the development of a large European medicines market. [Pg.125]

In Europe, inspections are conducted by Member States on behalf of the European Union. For drugs approved under the centralized procedure, inspections are coordinated by the European Agency for the Evaluation of Medicinal Products (EMEA refer to Sections 7.3 and 8.3.2). For countries that are members of the Pharmaceutical Inspection Cooperation Scheme (PIC/S Section 7.10), there is mutual recognition of inspections performed by members. [Pg.258]

Chapter V compliance and good clinical practice inspections, which, it is envisaged, will be coordinated by the European Agency for the Evaluation of Medicines (EMEA). [Pg.342]


See other pages where European Medicines Evaluation Agency inspections is mentioned: [Pg.37]    [Pg.555]    [Pg.126]    [Pg.70]    [Pg.27]    [Pg.29]    [Pg.300]   
See also in sourсe #XX -- [ Pg.140 ]




SEARCH



European Medicinal Evaluation Agency

European Medicines

European Medicines Evaluation

European Medicines Evaluation Agency

Inspections European

© 2024 chempedia.info