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European Banking Authority and European Medicines Agency after Brexit - Commission assessment of country offers
European Commission publishes assessment of Member State offers to host European Banking Authority and European Medicines Agency after Brexit
SMi Group
The SMi Group is a highly Professional, Independent and Global company that specialises in the production of Business-to-Business Conferences, Workshops and ...
Assessing illicit drugs in wastewater: advances in wastewater-based drug epidemiology
Assessing illicit drugs in wastewater: advances in wastewater-based drug epidemiology reviews a new approach to estimating drug use in populations, based on ...
Antimicrobial Resistance - guide
With about 25,000 patients dying per year in the EU from infections caused by drug resistant bacteria and related costs of over 1.5 billion euros in healthcare ...
EU probes Aspen price hikes for cancer drugs
The European Commission opened Monday a formal investigation into concerns that Aspen Pharma has engaged in excessive pricing concerning five life-saving ...
Joint purchasing of vaccines and medicines
The European Commission has approved a Joint Procurement Agreement, which will enable all EU countries to procure pandemic vaccines and other medical ...
The European Medicines Agency (EMA) has published additional guidance to help pharmaceutical companies prepare for the United Kingdom’s (UK) withdrawal from ...
The Committee for Medicinal Products for Human Use (CHMP) is responsible for preparing the European Medicines Agency's opinions on all questions concerning ...
Pharmaceuticals Unit: Contacts
Protecting the legal supply chain against counterfeited medicines - briefing
The European Commission has proposed today to protect the legal distribution chain from the infiltration of fake medicines. This is aimed at helping to ensure ...
Key directives: The EU Transparency Directive in the Pharmaceuticals sector
The EU Transparency Directive lays down harmonised provisions to ensure the transparency of measures adopted by national authorities to regulate the pricing ...
Drug facts, figures and analyses: across Europe and by country - Latest trends and legal, political, social and health responses - Selected issues: Drugs and ...
Since 1985, a score of European Community directives have been adopted with the aim of achieving a single, EU-wide market for pharmaceuticals.
The European Agency for the Evaluation of Medicinal Products (EMEA) is a decentralised body of the European Union. It has its headquarters in London since ...
Funding opportunities in the EU pharmaceutical industry
Expand your business in the pharmaceutical industry through the Entrepreneurship and Innovation Programme developed by the European Commission to support ...
Future direction of EU policy: innovation
Research and development (R&D) in life sciences is a precondition to pharmaceutical innovation. The Commission recognises the key role pharmaceutical R&D ...
The ICT Policy Support Programme (or ICT PSP) aims at stimulating innovation and competitiveness through the wider uptake and best use of ICT by citizens, ...
Information Communication Technologies Policy Support Programme (ICT PSP)
The ICT Policy Support Programme (or ICT PSP) aims at stimulating innovation and competitiveness through the wider uptake and best use of ICT by citizens, ...
The Innovative Medicines Initiative is a proposed partnership between the European Commission and the European Federation of Pharmaceutical Industry and ...
The EU and International Cooperation in Pharmaceuticals
The European Commission is an active member of the World Health Organisation’s International Medical Products Task Force (IMPACT). IMPACT counts all the major ...
The Rules Governing Medicinal Products in the European Union
The body of European Union legislation in the pharmaceutical sector is compiled in Volume 1 and Volume 5 of the publication “The rules governing medicinal ...
Infectious diseases are responsible for almost half of all deaths in developing countries, and half of these diseases are caused by HIV (AIDS), tuberculosis ...
European Community register of medicinal products for human use
EU Pharmaceutical Regulation: The Politics of Policy-making (European Policy Studies) (Amazon, Hardcover)
This book provides an analysis of European Union pharmaceutical regulation from a policy-making perspective. It focuses on how the conflicting agendas of the ...
Forum assesses competitiveness of Europe's pharmaceutical industry
Europe's Pharmaceutical Forum has concluded its three-year process and, on 2 October, put forward several recommendations addressing the many challenges facing ...
Pharmaceutical Medicine, Biotechnology and European Law (Amazon, Hardcover)
European law has been faced with increasingly complex issues emerging from rapid developments in pharmaceutical medicine and biotechnology. A team of ...
Pharmaceutical products
This Statistics in Focus presents price level indices for pharmaceutical products for 33 European countries in 2005. Price levels vary between more than 80% ...
Pharmaceuticals in the EU
European Union action in the pharmaceutical products sector is basically composed of two types of measures relating to industrial policy and the smooth ...
Strengthening pharmacovigilance to reduce adverse effects of medicines - briefing
Medicinal products contribute considerably to the health of EU citizens. They can, however, also have adverse effects. It is estimated that 5% of all hospital ...
Information to patients on prescription-only medicinal products - briefing
Citizens of the European Union have become more empowered and proactive consumers of healthcare, increasingly seeking information about medicines and ...
EU Alerts

EUbusiness Week no. 850
MEPs return to Brexit agenda
→ EUbusiness Week archive

The Week Ahead no. 446
UN Summit on Climate Action - regional seminar for candidate countries - European Week of Sport

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