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 Date: 2016-07-20 07:22:57Clinical research Pharmaceutical industry Clinical data management Drug safety Electronic common technical document Supplementary protection certificate European Medicines Agency Summary of Product Characteristics Pharmacovigilance Validation Drug Master File |
| Trial results: Modalities and timing of posting VersionAprilInterventional Clinical Trials that ended on or after 21 Julyi.e. the date of finalisation of the programming according to Commission GuiDocID: 1r4sk - View Document |
| emea_strap_url_cmyk_rev_en_std_cent.eps MASTERDocID: 1qVx6 - View Document |
| Question Q202 National Group: Sweden Suède Schweden Title:DocID: 1qeRN - View Document |
| B.12 AF user guide consolidated vet version EMADocID: 1pz2w - View Document |
| DOC DocumentDocID: 1oZjJ - View Document |