The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in London. It began operating in 1995. The Agency is responsible for the scientific evaluation, supervision and safety monitoring of medicines developed by pharmaceutical companies for use in the EU.
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General Database Information
European Medicines Agency (EMA-EUROPA)
Topic: Information on drugs and diseases
The Medical Research Council
The MRC ethics series document ‘Good research practice: principles and guidelines’ sets out the MRC’s expectations for MRC research units and institutes, MRC university units, MRC centres and MRC grant holders in the form of principles, guidelines and standards to foster good research practice in all MRC-funded research.
Topic: Information on drugs and diseases
Species specific
Guidance on Cephalopods
Topic: Cephalopod
Felasa Guidance For The Care and Welfare of Cephalopods in Research
Topic: Cephalopod
Cephalopods in Neuroscience: Regulations, Research and the 3Rs
Topic: Cephalopod
Guidelines for the Care and Welfare of Cephalopods in Research
A consensus based on an initiative by CephRes, FELASA and the Boyd Group.
Topic: Cephalopod