{"id":1425,"date":"2017-08-04T12:56:49","date_gmt":"2017-08-04T12:56:49","guid":{"rendered":"http:\/\/www.aaravinfotech.us\/biospherecro\/?page_id=1425"},"modified":"2026-10-07T16:17:42","modified_gmt":"2026-10-07T10:47:42","slug":"e-prudent","status":"publish","type":"page","link":"https:\/\/www.biospherecro.com\/e-prudent\/","title":{"rendered":"E-Prudent"},"content":{"rendered":"

[vc_row][vc_column][vc_custom_heading text=”… Revolutionizing clinical trials<\/strong>” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes”][vc_column_text]In our endeavour to speed up the process of clinical trials and make them cost effective while improving accuracy and transparency, we realised that work load of those who conduct trials [Project managers, Clinical Research Associates (CRAs)] gets extremely tedious with the limitations of distance (onsite physical monitoring), time, and communication. These limitations directly affect the decision making and trial performance consequently the quality of data generated. So, we came up with \u2018Wise and Precise\u2019e-Prudent that has revolutionised our clinical trials.<\/p>\n

e-Prudent<\/strong> is a comprehensive e-platform for remote monitoring and Interactive Web Response System (IWRS).[\/vc_column_text][\/vc_column][\/vc_row][vc_row bg_type=”no_bg”][vc_column][vc_separator gap=”tall” color=”custom” gradient=”yes”][\/vc_column][\/vc_row][vc_row][vc_column][vc_custom_heading text=”How e-Prudent Revolutionizes Clinical Trials<\/strong>” font_container=”tag:h2|text_align:center” use_theme_fonts=”yes” dsc_skin=”” dsc_typewriter=”” dsc_stroke=”” stroke_wd=”” dsc_bd=”” dsc_focus_on_slide=”” dsc_animation=”” animation_type=”” dsc_flt_img=”” dsc_flt_clr=”” dsc_flt_scroll=”” css_params=””][\/vc_column][\/vc_row][vc_row bg_type=”no_bg”][vc_column width=”1\/2″][vc_column_text el_class=”featured lead”]<\/p>\n

IWRS<\/strong><\/p>\n

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