{"id":9011,"date":"2025-01-03T11:14:41","date_gmt":"2025-01-03T10:14:41","guid":{"rendered":"https:\/\/czecrin.cz\/ks-implementation-unit-ctc\/"},"modified":"2025-05-09T11:48:25","modified_gmt":"2025-05-09T09:48:25","slug":"ks-implementation-unit-ctc","status":"publish","type":"page","link":"https:\/\/czecrin.cz\/en\/expertise-and-services\/ks-implementation-unit-ctc\/","title":{"rendered":"KS Implementation Unit (CTC)"},"content":{"rendered":"

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CLINICAL TRIALS CENTRE (CTC)<\/h1>\n

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More about CTC<\/h3>\n

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Clinical Trials are an integral and important part of a drug’s life cycle. During their implementation, it is necessary to comply with the legislation of the Czech Republic and the rules of Good Clinical Practice (GCP).<\/p>\n

The expert team of the CZECRIN Clinical Trials Unit provides comprehensive and partial services, including consultations and training, for the implementation of academic\/non-commercial clinical trials and research in\u00a0the field of pharmaceuticals, diagnostic methods and medical devices in\u00a0accordance with the legislation of the Czech Republic and GCP.<\/p>\n

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LIST OF ACTIVITIES<\/h3>\n

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Study Sponsor Responsibilities and Clinical Trial Project Management<\/p>\n

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Preparing Clinical Trials Documentation and Application and Medical Writer\/Medical Consultant Services<\/p>\n

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Clinical Trial Regulatory Authority (S\u00daKL) and Ethics Committee Submission<\/p>\n

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Data management and biostatistics<\/p>\n

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Pharmacovigilance<\/p>\n

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Monitoring <\/p>\n

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Consulting and Expert’s Advisory<\/p>\n

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Educational Activities<\/span><\/span><\/p>\n

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LIST OF ACTIVITIES<\/h3>\n

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Study Sponsor Responsibilities and Clinical Trial Project Management<\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.27.4″ _module_preset=”default” background_color=”#FFFFFF” custom_margin=”||12px||false|false” custom_padding=”|||30px|false|false” border_radii=”on|6px|6px|6px|6px” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.4″ _module_preset=”default” text_font=”|600|||||||” text_text_color=”#2948F1″ custom_padding=”||||false|true” custom_padding_tablet=”||||false|true” custom_padding_phone=”||||false|true” custom_padding_last_edited=”on|phone” background_color_tablet=”#FFFFFF” background_last_edited=”on|tablet” background_enable_color_tablet=”off” border_radii_tablet=”on|6px|6px|6px|6px” border_radii_phone=”on|6px|6px|6px|6px” border_radii_last_edited=”on|phone” global_colors_info=”{}”]<\/p>\n

Preparing Clinical Trials Documentation and Application and Medical Writer\/Medical Consultant Services<\/p>\n

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Clinical Trial Regulatory Authority (S\u00daKL) and Ethics Committee Submission<\/p>\n

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Data management and biostatistics<\/p>\n

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Pharmacovigilance<\/p>\n

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Monitoring <\/p>\n

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Consulting and Expert’s Advisory<\/p>\n

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Educational Activities<\/span><\/span><\/p>\n

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Comprehensive summary of information about the Clinical Trials Implementation Unit<\/p>\n

Download<\/a><\/strong><\/p>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” animation_style=”slide” animation_direction=”right” global_colors_info=”{}”][et_pb_blurb title=”CTC Projects” image=”https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/01\/datab-1.webp” image_icon_width=”24%” icon_alignment=”left” icon_alignment_tablet=”center” icon_alignment_phone=”center” icon_alignment_last_edited=”on|tablet” _builder_version=”4.27.4″ _module_preset=”default” header_level=”h2″ header_line_height=”1.6em” custom_padding=”98px||||false|false” custom_padding_tablet=”98px||30px||false|false” custom_padding_phone=”98px||||false|false” custom_padding_last_edited=”on|tablet” hover_enabled=”0″ text_orientation_tablet=”center” text_orientation_phone=”center” text_orientation_last_edited=”on|tablet” global_colors_info=”{}” sticky_enabled=”0″]<\/p>\n

Complete database of projects and studies that have benefited from CZECRIN expertise<\/p>\n

Under Construction<\/strong><\/p>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” background_enable_color=”off” background_image=”https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/01\/F_Obr-1.jpg” custom_padding=”100px|30px|30px|30px|false|true” animation_style=”slide” animation_direction=”right” global_colors_info=”{%22gcid-c01695cd-def2-49cb-9935-1d80b38bf4e2%22:%91%22background_color%22%93}”][et_pb_blurb title=”I’m intereseted in\u00a0co-operation” image=”https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/01\/postava.webp” image_icon_width=”30%” _builder_version=”4.27.4″ _module_preset=”default” header_level=”h3″ text_orientation=”center” background_layout=”dark” global_colors_info=”{}”]<\/p>\n

We\u00a0offer our expertise to\u00a0assist in\u00a0the implementation of your project.<\/p>\n

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CLINICAL TRIALS CENTRE (CTC)More about CTCClinical Trials are an integral and important part of a drug’s life cycle. 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