Examples of 'european medicines agency' in a sentence
Meaning of "european medicines agency"
The European Medicines Agency (EMA) is a regulatory body responsible for evaluating and supervising medicinal products within the European Union (EU). It ensures that medicines are safe, effective, and of high quality through scientific assessments and ongoing monitoring
                                                                                            How to use "european medicines agency" in a sentence
                                        
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                                european medicines agency
                                
                                
                                
                            
                            
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Changing the european medicines agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Annex ii scientific conclusions and grounds for positive opinion presented by the european medicines agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The european medicines agency responsibilities and administrative structure.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Paediatric working party of the european medicines agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency publishes report on patient recruitment and geographical location of clinical trials.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    A framework for extrapolation is currently being finalized by the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency started a review of emergency contraceptives.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    This report consists of a reminder of what the European Medicines Agency should be.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency recommends restricting the use of modafinil.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Completion of the bid to host the headquarters of the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency gives recommendations on use of intravenous nicardipine.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Detailed information on this medicine is available on the European Medicines Agency web site.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency simplifies processing of fee reductions for orphan medicines.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Conclusions on the granting of the conditional marketing authorisation presented by the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency increases transparency of ongoing applications for human medicines.
                                        
                                    See also
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Scientific conclusions and grounds for positive opinion presented by the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency updates on the review of Pandemrix and reports of narcolepsy.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Corresponding applications for both medicines have been filed with the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency is also currently reviewing a marketing application for romosozumab.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Lyxumia is the proprietary name approved by the European Medicines Agency and other health authorities.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency starts a review of nasal and mouth sprays containing fusafungine.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Scientific conclusions and grounds for refusal and suspension presented by the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency has completed a review of the safety and effectiveness of modafinil.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Scientific conclusions and grounds for refusal of the variation presented by the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency has completed a review of the safety and effectiveness of fibrates.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The company has also applied for orphan drug designation from the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency has completed a review of the safety and effectiveness of bufexamac.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    At the request of the European Medicines Agency PSURs.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency charges pharmaceutical companies fees for the services it provides.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    System of fees payable to the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency has completed a review of the safety and effectiveness of benfluorex.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    I voted to grant discharge to the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency has completed a review of the safety and effectiveness of dexrazoxane.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    It is classified as a rare disease by the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency boosts EU transparency with online publication of suspected side effect reports.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Finland is an excellent place for European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency recommended restricting the use of modafinil for narcolepsy only.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    It is currently under review by the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency has waived the obligation to submit the results of studies.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    A single application to the European Medicines Agency will suffice.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency can not accept side effect reports directly from patients.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Abiraterone acetate was also licensed by the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency has recognized that motherwort helps relieve symptoms of nervous tension.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Copenhagen is a significant contender to host the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    The European Medicines Agency must fulfil its transparency obligations and resist industry pressure.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    National websites are listed with the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency update on combined contraceptives.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Summary of the annual report of the European Medicines Agency.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    European Medicines Agency releases adverse reaction reports.
                                        
                                    
                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                                    Read more at the website of the European Medicines Agency.
                                        
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                                                            The travel agency would be first base
                                                        
                                                    
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                                                            And my agency has not fallen apart
                                                        
                                                    
                                        Examples of using European
                                        
                                                                                            
                                                    
                                                        
                                                        
                                                    
                                                         
                                                        
                                                                                                            
                                                
                                                                                            
                                                    
                                                        
                                                        
                                                    
                                                         
                                                        
                                                                                                            
                                                
                                                                                            
                                                    
                                                        
                                                        
                                                    
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                                                            Conference of european statisticians commission of the european
                                                        
                                                    
                                                            Statistical commission and commission of the european
                                                        
                                                    
                                                            European association of hotel and tourism schools
                                                        
                                                    
                                        Examples of using Medicines
                                        
                                                                                            
                                                    
                                                        
                                                        
                                                    
                                                         
                                                        
                                                                                                            
                                                
                                                                                            
                                                    
                                                        
                                                        
                                                    
                                                         
                                                        
                                                                                                            
                                                
                                                                                            
                                                    
                                                        
                                                        
                                                    
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                                                            Keep all medicines out of reach of children
                                                        
                                                    
                                                            There is no interruption of programs to develop new medicines
                                                        
                                                    
                                                            Viscous medicines may also require dilution