[vc_section bklyn_overlay=”true” background_position=”center center” section_separator_bottom=”true” section_separator_bottom_zindex=”true” section_separator_svg_bottom=”curve” section_separator_bottom_flip=”true” section_separator_bottom_hide_on_tablet=”” section_separator_bottom_hide_on_mobile=”” el_name=”First Section” css=”.vc_custom_1560385751862{margin-top: 30px !important;margin-right: 30px !important;margin-bottom: 0px !important;margin-left: 30px !important;border-bottom-width: 0px !important;padding-top: 0px !important;padding-bottom: 0px !important;background-image: url(https://weareinfinite.mx/wp-content/uploads/2019/06/infinite-clinical-registros-sanitarios-comercializacion-1.jpg?id=4164) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}” section_separator_bottom_color_1=”#2c2c2c” bklyn_overlay_color=”rgba(255, 255, 255, 0.8)”][vc_row full_width=”stretch_row_content_no_spaces” css=”.vc_custom_1560385764413{padding-top: 0px !important;}”][vc_column width=”1/3″ css=”.vc_custom_1560385693753{padding-top: 30px !important;padding-right: 30px !important;padding-bottom: 30px !important;padding-left: 30px !important;}” offset=”vc_col-lg-4 vc_col-md-4 vc_col-sm-4 vc_col-xs-12 vc_hidden-xs”][ut_accordion easing=”linear” transition=”300″ count=”no” label_font_size=”15″ css=”.vc_custom_1564681675196{padding-top: 5px !important;padding-right: 15px !important;padding-bottom: 5px !important;padding-left: 15px !important;background-color: rgba(255, 255, 255, 0.86) !important;*background-color: rgba(255,255, 255, 0.86) !important;}” class=”menu-accordion” label_color=”#0a0a0a” text_color=”#81d742″][ut_accordion_item label=”Regulatory Affairs”]
Submission of information for ethics committees
[/ut_accordion_item][ut_accordion_item open=”true” label=”Clinical Operations”]
[/ut_accordion_item][ut_accordion_item label=”Research Products Storage/Depot”]
Integral management of research products
[/ut_accordion_item][ut_accordion_item label=”Health records before COFEPRIS”]
Requirements of the Mexican regulations
[/ut_accordion_item][ut_accordion_item open=”true” label=”Consulting Services”]
[/ut_accordion_item][ut_accordion_item label=”Complementary Services”]
[/ut_accordion_item][ut_accordion_item label=”Pharmacovigilance / Technovigilance”]
[/ut_accordion_item][ut_accordion_item label=”Business Solutions”]
Preparation of documents for research
Research protocols for medical devices
Research protocols in cosmetics
Import of products of research
Compliance with labelling rules
[/ut_accordion_item][ut_accordion_item label=”Training”]
[/ut_accordion_item][/ut_accordion][/vc_column][vc_column width=”1/2″ offset=”vc_col-lg-offset-0 vc_col-lg-6 vc_col-md-8 vc_col-sm-8 vc_col-xs-12″ css=”.vc_custom_1560385757636{padding-right: 30px !important;padding-left: 30px !important;}”][ultimate_spacer height=”150″ height_on_tabs=”150″ height_on_tabs_portrait=”0″ height_on_mob_landscape=”0″ height_on_mob=”0″][ultimate_heading main_heading=”Consulting Services” heading_tag=”h1″ main_heading_color=”#373c48″ sub_heading_color=”#373c48″ main_heading_font_size=”desktop:52px;tablet:52px;tablet_portrait:40px;mobile_landscape:40px;mobile:30px;” main_heading_style=”font-weight:bold;” main_heading_margin=”margin-bottom:30px;” sub_heading_font_size=”desktop:18px;” sub_heading_line_height=”desktop:30px;”][/ultimate_heading][vc_column_text]
In INFINITE we work linked with all our clients, in this way we identify the best processes for the execution of each of the activities within your clinical research project or support for required regulatory issues. In this way, through effective communication, we support our clients to know the environment, the industry and the market, which will allow them to obtain a holistic view of the whole panorama for the registration of new clinical research protocols, compliance with all the requirements of the legal framework for the registration of new products, drugs and medical devices, as well as consulting in the new legal framework for pharmacovigilance or techno-surveillance regulations, for companies that sell or manufacture medicines or medical devices.
[/vc_column_text][ut_btn button_effect=”winona” button_size=”bklyn-btn-small” button_custom_border=”yes” button_border_width=”2″ font_family=”inherit” font_weight=”” button_text=”Empezar” button_text_color=”#474b54″ button_background=”transparent” button_border_color=”#004d72″ spacing=”padding-top:15px;padding-right:40px;padding-bottom:15px;padding-left:40px” button_link=”url:%23how-can-we-help-you|||” effect=”fadeIn”][/vc_column][/vc_row][vc_row full_width=”stretch_row_content_no_spaces” hide_on_desktop=”true” hide_on_tablet=”true” css=”.vc_custom_1554832684299{margin-top: 0px !important;margin-bottom: 0px !important;padding-top: 0px !important;padding-bottom: 0px !important;background-color: #ffffff !important;}”][vc_column offset=”vc_col-lg-offset-0 vc_col-lg-12 vc_col-md-12 vc_col-sm-12 vc_col-xs-12″ css=”.vc_custom_1554832549540{margin-top: 0px !important;margin-bottom: 0px !important;padding-right: 30px !important;padding-left: 30px !important;background-color: #ffffff !important;}”][ut_accordion easing=”linear” transition=”300″ count=”no” label_font_size=”15″ css=”.vc_custom_1564681675196{padding-top: 5px !important;padding-right: 15px !important;padding-bottom: 5px !important;padding-left: 15px !important;background-color: rgba(255, 255, 255, 0.86) !important;*background-color: rgba(255,255, 255, 0.86) !important;}” class=”menu-accordion” label_color=”#0a0a0a” text_color=”#81d742″][ut_accordion_item label=”Regulatory Affairs”]
Submission of information for ethics committees
[/ut_accordion_item][ut_accordion_item open=”true” label=”Clinical Operations”]
[/ut_accordion_item][ut_accordion_item label=”Research Products Storage/Depot”]
Integral management of research products
[/ut_accordion_item][ut_accordion_item label=”Health records before COFEPRIS”]
Requirements of the Mexican regulations
[/ut_accordion_item][ut_accordion_item open=”true” label=”Consulting Services”]
[/ut_accordion_item][ut_accordion_item label=”Complementary Services”]
[/ut_accordion_item][ut_accordion_item label=”Pharmacovigilance / Technovigilance”]
[/ut_accordion_item][ut_accordion_item label=”Business Solutions”]
Preparation of documents for research
Research protocols for medical devices
Research protocols in cosmetics
Import of products of research
Compliance with labelling rules
[/ut_accordion_item][ut_accordion_item label=”Training”]
[/ut_accordion_item][/ut_accordion][ultimate_spacer height=”” height_on_mob=”70″][/vc_column][/vc_row][/vc_section][vc_section background_attachment=”fixed” section_separator_top=”true” section_separator_top_zindex=”true” section_separator_svg_top=”curve” section_separator_top_flip=”true” section_separator_top_hide_on_tablet=”” section_separator_top_hide_on_mobile=”” section_separator_top_color_1=”#2c2c2c” css=”.vc_custom_1564684917020{padding-top: 0px !important;padding-bottom: 0px !important;}” el_id=”how-can-we-help-you”][vc_row section_separator_bottom=”true” section_separator_svg_bottom=”curve” section_separator_bottom_flip=”true” section_separator_bottom_hide_on_tablet=”” section_separator_bottom_hide_on_mobile=”” section_separator_bottom_color_1=”#004d72″ css=”.vc_custom_1560386384600{background-color: #004d72 !important;}”][vc_column][ultimate_heading main_heading=”How can we help you?” heading_tag=”h3″ main_heading_color=”#ffffff” main_heading_font_size=”desktop:45px;tablet:40px;tablet_portrait:40px;mobile_landscape:22px;mobile:22px;” main_heading_style=”font-weight:bold;”][/ultimate_heading][/vc_column][/vc_row][vc_row full_height=”yes” equal_height=”yes” content_placement=”middle” bklyn_overlay=”true” parallax=”content-moving” section_separator_top=”true” section_separator_top_zindex=”true” section_separator_svg_top=”curve” section_separator_top_flip=”true” section_separator_top_hide_on_tablet=”” section_separator_top_hide_on_mobile=”” section_separator_top_color_1=”#004d72″ css=”.vc_custom_1560385990258{margin-top: 0px !important;padding-bottom: 15px !important;background-image: url(https://weareinfinite.mx/wp-content/uploads/2019/06/infinite-clinical-consultoria.jpeg?id=4170) !important;background-position: center;background-repeat: no-repeat !important;background-size: cover !important;}” bklyn_overlay_color=”linear-gradient(to top, rgba(0, 0, 0, 0.86) 0%, rgba(0, 0, 0, 0.7) 100%)”][vc_column offset=”vc_col-lg-12 vc_col-md-12 vc_col-sm-11 vc_col-xs-12″][vc_column_text]Our quality standards, our wide portfolio of services and our unique flexibility in the market, allow us to offer you a professional and personalized service that we are sure will meet your expectations:
Our consulting services include:[/vc_column_text][vc_row_inner equal_height=”yes” gap=”5″][vc_column_inner width=”1/4″ offset=”vc_col-xs-6″][vc_icon icon_fontawesome=”fa fa-check” color=”white” align=”center” css=”.vc_custom_1560386072235{margin-bottom: 25px !important;}”][ut_custom_heading tag=”p” align=”center” font_size=”20″ color=”#ffffff” css=”.vc_custom_1564520723212{margin-bottom: 10px !important;}”]Regulatory framework for medicines[/ut_custom_heading][/vc_column_inner][vc_column_inner width=”1/4″ offset=”vc_col-xs-6″][vc_icon icon_fontawesome=”fa fa-check” color=”white” align=”center” css=”.vc_custom_1560386072235{margin-bottom: 25px !important;}”][ut_custom_heading tag=”p” align=”center” font_size=”20″ color=”#ffffff” css=”.vc_custom_1564520734692{margin-bottom: 10px !important;}”]Regulatory framework for medical devices[/ut_custom_heading][/vc_column_inner][vc_column_inner width=”1/4″ offset=”vc_col-xs-6″][vc_icon icon_fontawesome=”fa fa-check” color=”white” align=”center” css=”.vc_custom_1560386072235{margin-bottom: 25px !important;}”][ut_custom_heading tag=”p” align=”center” font_size=”20″ color=”#ffffff” css=”.vc_custom_1564520743230{margin-bottom: 10px !important;}”]Regulatory framework for food supplements[/ut_custom_heading][/vc_column_inner][vc_column_inner width=”1/4″ offset=”vc_col-xs-6″][vc_icon icon_fontawesome=”fa fa-check” color=”white” align=”center” css=”.vc_custom_1560386072235{margin-bottom: 25px !important;}”][ut_custom_heading tag=”p” align=”center” font_size=”20″ color=”#ffffff” css=”.vc_custom_1564520760186{margin-bottom: 10px !important;}”]Import of inputs for clinical research[/ut_custom_heading][/vc_column_inner][vc_column_inner width=”1/12″ offset=”vc_col-lg-1 vc_col-md-1 vc_col-sm-1 vc_col-xs-1 vc_hidden-xs”][/vc_column_inner][vc_column_inner width=”1/4″ offset=”vc_col-xs-6″][vc_icon icon_fontawesome=”fa fa-check” color=”white” align=”center” css=”.vc_custom_1560386072235{margin-bottom: 25px !important;}”][ut_custom_heading tag=”p” align=”center” font_size=”20″ color=”#ffffff” css=”.vc_custom_1564520770863{margin-bottom: 10px !important;}”]Development of clinical research protocols[/ut_custom_heading][/vc_column_inner][vc_column_inner width=”1/4″ offset=”vc_col-xs-6″][vc_icon icon_fontawesome=”fa fa-check” color=”white” align=”center” css=”.vc_custom_1560386072235{margin-bottom: 25px !important;}”][ut_custom_heading tag=”p” align=”center” font_size=”20″ color=”#ffffff” css=”.vc_custom_1564520786976{margin-bottom: 10px !important;}”]Pharmacovigilance and technovigilance[/ut_custom_heading][/vc_column_inner][vc_column_inner width=”1/4″ offset=”vc_col-xs-6″][vc_icon icon_fontawesome=”fa fa-check” color=”white” align=”center” css=”.vc_custom_1560386072235{margin-bottom: 25px !important;}”][ut_custom_heading tag=”p” align=”center” font_size=”20″ color=”#ffffff” css=”.vc_custom_1564520796991{margin-bottom: 10px !important;}”]Conditioning medication for research[/ut_custom_heading][/vc_column_inner][/vc_row_inner][/vc_column][/vc_row][/vc_section]