In response to the public consultation on "Key ideas for better protection of patients against the risk of counterfeit medicines", the Commission received 123 contributions from stakeholders. Of th
read more » Discuss Add this link to...Bury Add to:
| Bookmarks
The European Commission (EC), the European Medicines Agency (EMEA) and the United States Food and Drug Administration (FDA) have affirmed their commitment to regulatory cooperation and to intensifyin
read more » Discuss Add this link to...Bury Add to:
| Bookmarks
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 admissions are due to an adverse drug re
read more » Discuss Add this link to...Bury Add to:
| Bookmarks
The European Medicines Agency, the European Commission and Health Canada, the Canadian regulatory authority for medicines, have agreed on an implementation plan for their confidentiality arrangement.
read more » Discuss Add this link to...Bury Add to:
| Bookmarks