{"id":868,"date":"2021-02-12T10:27:47","date_gmt":"2021-02-12T09:27:47","guid":{"rendered":"https:\/\/ago-ovar.de\/services\/study-implementation\/"},"modified":"2021-12-08T13:41:31","modified_gmt":"2021-12-08T12:41:31","slug":"study-implementation","status":"publish","type":"page","link":"https:\/\/ago-ovar.de\/en\/services\/study-implementation\/","title":{"rendered":"Study Implementation"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; specialty=&#8221;on&#8221; _builder_version=&#8221;4.4.8&#8243; background_color=&#8221;#e0edf9&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;3_4&#8243; specialty_columns=&#8221;3&#8243; _builder_version=&#8221;3.25&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_row_inner _builder_version=&#8221;4.4.8&#8243; custom_padding=&#8221;||13px|||&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.4.8&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.4.8&#8243; text_text_color=&#8221;#000000&#8243; header_font=&#8221;|700||on|||||&#8221; header_text_color=&#8221;#11487E&#8221; header_2_text_color=&#8221;#11487E&#8221; custom_margin=&#8221;||21px|||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h1>Study Implementation<\/h1>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner _builder_version=&#8221;4.4.8&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;3_4&#8243; _builder_version=&#8221;4.4.8&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.4.8&#8243; text_text_color=&#8221;#000000&#8243; text_font_size=&#8221;16px&#8221; header_text_color=&#8221;#11487E&#8221; header_2_text_color=&#8221;#11487E&#8221; header_2_font_size=&#8221;24px&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p>During the term of a clinical trial, the following services are rendered (no exhaustive list):<\/p>\n<p>&nbsp;<\/p>\n<ul>\n<li> Preparation and distribution of the study documents<\/li>\n<li>Randomisation \/ registration<br \/> SAE\/SUSAR Management<\/li>\n<li>Preparing and obtaining approval from the competent\/accompanying Ethics Committee in case of subsequent content-related or formal modifications<\/li>\n<li>Preparation and submission of Annual Safety Reports (ASRs) to the competent federal authorities including obtaining approvals of subsequent modifications<\/li>\n<li>Scientific and operative support to the trial centres<\/li>\n<li>Monitoring<\/li>\n<li>Follow up<\/li>\n<\/ul>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][\/et_pb_column][et_pb_column type=&#8221;1_4&#8243; 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