ICH
The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) is unique in bringing together the regulatory authorities and pharmaceutical industry of Europe, Japan and the US to discuss scientific and technical aspects of drug registration. ICH's mission is to achieve greater harmonisation to ensure that safe, effective, and high quality medicines are developed and registered in the most resource-efficient manner. Click here
WHO
WHO, World Health Organization, is the directing and coordinating authority for health within the United Nations system. It is responsible for providing leadership on global health matters, shaping the health research agenda, setting norms and standards, articulating evidence-based policy options, providing technical support to countries and monitoring and assessing health trends. Click here
ClinRegs
The NIAID ClinRegs website provides an online database of country-specific clinical research regulatory information designed to enable users to explore regulations within a country and compare requirements across countries. By providing well-documented, up-to-date regulatory information for multiple countries in a single place, ClinRegs is intended to serve as a central resource and time-saver for persons involved in planning and implementing international clinical research. ClinRegs’ easy-to-navigate functionality enables users to obtain a digestible overview of a country’s regulatory requirements related to a specific topic and to compare requirements across multiple countries. Click here
01
02
03
Drug Information Association
The Drug Information Association (DIA) was founded in 1964 by a group of 30 pharmaceutical professionals, medical writers and academicians who saw the need to facilitate communications and foster cooperative efforts among professionals working in health care industries primarily engaged in drug development, medical communications and health information. DIA offers a large selection of meetings, webinars, e-learning and training programs throughout the world. The Association also provides three regular publications to its members including: The Global Forum, a news and information digital resource that keeps members advised of activities and events at the Association as well as current trends in the health care arena; Therapeutic Innovation & Regulatory Science, DIA’s official scholarly, peer-reviewed journal; and the CSO Directory, an annual, international digital reference guide compiling information from drug development and clinical trial companies. Click here