Eurotrials works in conjunction with local operation centres or in partnership with other companies in Europe from its base in Portugal.
Its experienced, multidisciplinary team is one of its main success factors in developing, implementing and managing multinational studies.
Where regulation and pharmacovigilance are concerned, procedures and requirements are becoming more and more global, which is why Eurotrials has developed the necessary competences to assist its customers and partners (including those in Latin America) in dealings with the EMEA, European Medicines Agency.
Its experienced, multidisciplinary team is one of its main success factors in developing, implementing and managing multinational studies.
European Directive 2001/20/EC, which has been progressively applied in all European Union countries, has standardised regulatory procedures in the implementation of clinical trials.
This, plus Eurotrials’ collaboration with networks of clinical research centres of excellence , enables it to involve top teams in its projects in different countries in Europe.
This, plus Eurotrials’ collaboration with networks of clinical research centres of excellence , enables it to involve top teams in its projects in different countries in Europe.
Where regulation and pharmacovigilance are concerned, procedures and requirements are becoming more and more global, which is why Eurotrials has developed the necessary competences to assist its customers and partners (including those in Latin America) in dealings with the EMEA, European Medicines Agency.
Inęs Pedroso da Costa, Catarina Alves, Pedro Aguiar, Catarina Silva, Pedro Noronha
