What is a Clinical Trial? A Clinical Trial is a study performed to investigate the safety or efficacy of a medicine. For human medicines, these studies are carried out in human volunteers. The Clinical Trial Portal and IDMP SPORS EMA’s new Clinical Trials Portal...
Note: Meet IDMP1 Partner Dieter Schlaps at the RSIDM in North Bethesda Feburary 5-7, 2018 IDMP1 will be present at the upcoming Regulatory Submissions, Information and Document Management Form (RSIDM), at North Bethesda (US), from February 5-7, 2018. If you are there,...
EMA´s landingpage IDMP on implementation of International Organization for Standardization (ISO) identification of medicinal products (IDMP) standards has been launched. There are described the common standards, formats and terminologies which should be used in...
The European Medicines Agency (EMA) has published a guide to support the implementation of a new international standard for the safety monitoring of medicines in the European Union (EU). The so-called ISO ICSR standard improves the reporting of suspected side effects...
Match your data with IDMP controlled terms
The Identification for Medicinal Products (IDMP) translating and converting tool for healthcare professionals.
