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</html><description>[vc_row padding_top=&#x201D;30&#x2033; padding_bottom=&#x201D;10&#x2033;][vc_column][vc_separator color=&#x201D;custom&#x201D; align=&#x201D;align_left&#x201D; border_width=&#x201D;2&#x2033; el_width=&#x201D;10&#x2033; accent_color=&#x201D;#a1bf3b&#x201D; css=&#x201D;.vc_custom_1635368107018{margin-bottom: 1px !important;padding-bottom: 5px !important;}&#x201D;][vc_custom_heading text=&#x201D;Advice and regulatory support for COFEPRIS&#x201D; font_container=&#x201D;tag:h2|font_size:35|text_align:left|color:%230d1250|line_height:1.5&#x2033; google_fonts=&#x201D;font_family:Montserrat%3Aregular%2C700|font_style:700%20bold%20regular%3A700%3Anormal&#x201D;][/vc_column][/vc_row][vc_row padding_top=&#x201D;20&#x2033;][vc_column width=&#x201D;1/2&#x2033;][vc_column_text] We have a team of experts with extensive experience in regulating biosimilar medicines that can advice you in the registration and approval process in the COFEPRIS. We focus on understanding the regulatory needs of the Mexican pharmaceutical [&hellip;]</description></oembed>
