Regulatory Agencies

        European Medicines Agency (EMEA)
                    (EMEA Documents & Drafts on Pharmacovigilance)
        Health Canada
        International Conference on Harmonisation (ICH)
                    (ICH Guidelines)
                    Electronic Standards for the Transfer of Regulatory Information (ESTRI)
        Medicines and Healthcare products Regulatory Agency (MHRA)
        U.S. Food and Drug Administration (FDA)
                    Adverse Event Reporting System (AERS)
                    AERS Electronic Submissions
                    Center for Drug Evaluation and Research (CDER)
                    MedWatch
        World Health Organization (WHO)
        Japanese Ministry of Health, Labour and Welfare

Trade Groups & Associations

        International Federation of Pharmaceutical Manufacturers Associations (IFPMA)
        Japan Pharmaceutical Manufacturers Association (JPMA)
                    JPMA (english)
        Pharmaceutical Manufacturers Association of Canada (PMAC)
        Pharmaceutical Research Manufacturers Association (PhRMA)

Scientific & Professional Groups

        Drug Information Association (DIA)
        Food, Drug, and Law Institute (FDLI)
        Regulatory Affairs Professional Society (RAPS)
        Society of Clinical Research Associates (SOCRA)
 

The links on this page have been provided for informational purposes only.
The information conveyed within these links are those of the individual organizations.