Neoclinus

Welcome to Neoclinus

We accelerate life-changing therapy development.

Global Contract Research Organization, supports leading pharmaceutical and bio-tech companies

About

About Neoclinus

Your trusted partner in Clinical Research excellence.

Neoclinus is a forward-thinking Global Contract Research Organization (CRO) deeply committed to quality. Our dedicated team supports top-tier pharmaceutical and bio-tech firms, as well as burgeoning enterprises, through a comprehensive suite of services.

With decades of collective experience in drug development, our senior leadership provides invaluable insights, guiding program-level strategies and project execution across diverse therapeutic domains.

At Neoclinus, we prioritize continuous staff development through rigorous training initiatives, innovative recruitment practices, and enriching career pathways. This commitment ensures that we attract and retain top talent, fostering a client-centric workforce that thrives across our global footprint.

Services

Our Services

Services We Offer

[difl_flipbox title_front=”Data Management” content_front=”

Neoclinus involves the collection, processing, and analysis of clinical trial data to ensure its accuracy, completeness, and regulatory compliance.

” title_back=”Data Management” content_back=”

The clinical data management team is involved in every aspect of the clinical trial process, from protocol development to report writing.

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[difl_flipbox title_front=”Statistical Programming” content_front=”

It plays a crucial role in analyzing and interpreting clinical trial data to support evidence-based decision-making and regulatory submissions.

” title_back=”Statistical Programming” content_back=”

Statistical Programming is a critical function in clinical research that involves the application of statistical methods to analyze data from clinical trials.

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[difl_flipbox title_front=”Pharmacovigilance” content_front=”

Pharmacovigilance is a critical component of regulatory affairs, dedicated to ensuring the safety and efficacy of pharmaceutical products throughout their lifecycle.

” title_back=”Pharmacovigilance” content_back=”With our deep expertise in ICSR processing, aggregate reporting, signal and risk management, and regulatory compliance, we are well-equipped to assist you.” fb_front_align=”center” fb_back_align=”center” fb_btn_button_text=”View Details” fb_btn_button_url=”@ET-DC@eyJkeW5hbWljIjp0cnVlLCJjb250ZW50IjoicG9zdF9saW5rX3VybF9wYWdlIiwic2V0dGluZ3MiOnsicG9zdF9pZCI6IjIyMCJ9fQ==@” fb_btn_button_url_new_window=”1″ fb_btn_button_align=”center” image_front_image=”https://neoclinus.com/wp-content/uploads/2024/06/Pharmacovigilance.png” image_front_image_align=”center” image_front_max_width=”30%” fb_animation=”slide” fb_slide_direction=”slide_up” fb_background_bgcolor=”RGBA(255,255,255,0)” fb_back_background_bgcolor=”#79c6f3″ fb_back_background_background_image=”https://neoclinus.com/wp-content/uploads/2024/06/flip-bg.png” container_margin=”0px|0px|0px|0px|true|true” container_padding=”0px|0px|0px|0px|true|true” front_wrapper_padding=”40px|40px|40px|40px|true|true” front_wrapper_padding_tablet=”30px|30px|30px|30px|true|true” front_wrapper_padding_phone=”20px|20px|20px|20px|true|true” front_wrapper_padding_last_edited=”on|tablet” back_wrapper_padding=”40px|40px|40px|40px|true|true” back_wrapper_padding_tablet=”30px|30px|30px|30px|true|true” back_wrapper_padding_phone=”20px|20px|20px|20px|true|true” back_wrapper_padding_last_edited=”on|tablet” img_container_front_margin=”||16px||false|false” img_container_front_margin_tablet=”||13px||false|false” img_container_front_margin_phone=”||10px||false|false” img_container_front_margin_last_edited=”on|tablet” img_container_front_padding=”||0px||false|false” title_front_margin=”||16px||false|false” title_front_margin_tablet=”||13px||false|false” title_front_margin_phone=”||10px||false|false” title_front_margin_last_edited=”on|tablet” title_front_padding=”||0px||false|false” title_back_margin=”||16px||false|false” title_back_margin_tablet=”||13px||false|false” title_back_margin_phone=”||10px||false|false” title_back_margin_last_edited=”on|tablet” title_back_padding=”||0px||false|false” text_back_margin=”||24px||false|false” text_back_margin_tablet=”||20px||false|false” text_back_margin_phone=”||15px||false|false” text_back_margin_last_edited=”on|tablet” button_padding=”0px|0px|0px|0px|true|true” _builder_version=”4.25.0″ _dynamic_attributes=”fb_btn_button_url” _module_preset=”default” title_font=”|600|||||||” title_text_align=”center” title_text_color=”#000000″ title_font_size=”24px” title_line_height=”28.8px” content_font=”||||||||” content_text_align=”center” content_text_color=”#000000″ content_font_size=”16px” content_line_height=”25.6px” title_back_font=”|600|||||||” title_back_text_align=”center” title_back_text_color=”#000000″ title_back_font_size=”24px” title_back_line_height=”28.8px” content_back_font=”||||||||” content_back_text_align=”center” content_back_text_color=”#000000″ content_back_font_size=”16px” content_back_line_height=”25.6px” button_font=”|700|||||||” button_text_align=”center” button_text_color=”#080808″ button_line_height=”24px” title_font_size_tablet=”22px” title_font_size_phone=”20px” title_font_size_last_edited=”on|tablet” content_font_size_tablet=”15px” content_font_size_phone=”14px” content_font_size_last_edited=”on|tablet” content_line_height_tablet=”25px” content_line_height_phone=”24px” content_line_height_last_edited=”on|tablet” title_back_font_size_tablet=”22px” title_back_font_size_phone=”20px” title_back_font_size_last_edited=”on|tablet” content_back_font_size_tablet=”15px” content_back_font_size_phone=”14px” content_back_font_size_last_edited=”on|tablet” content_back_line_height_tablet=”25px” content_back_line_height_phone=”24px” content_back_line_height_last_edited=”on|tablet” button_font_size_tablet=”15px” button_font_size_phone=”14px” button_font_size_last_edited=”on|tablet” custom_css_main_element=”font-weight: 400;” border_width_bottom_button_b=”1px” border_color_bottom_button_b=”#080808″ border_width_all_front=”1px” border_color_all_front=”RGBA(255,255,255,0)” border_width_all_back=”1px” border_color_all_back=”#7AC403″ locked=”off” global_colors_info=”{}” button_text_color__hover_enabled=”on|desktop” button_text_color__hover=”#15B212″][/difl_flipbox]

[difl_flipbox title_front=”Medical writing” content_front=”

It is a vital aspect of regulatory affairs, providing clear and accurate documentation required for the successful approval and marketing of pharmaceutical products and medical devices.

” title_back=”Medical writing” content_back=”

Medical writing services that meet the high demands of the regulatory processes involved in the development of drugs.

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[difl_flipbox title_front=”Medical Affairs & Strategy ” content_front=”

we are dedicated to advancing healthcare through our comprehensive Medical Affairs and Strategy services.

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Navigating the regulatory landscape for medical devices and in-vitro diagnostics (IVDs) requires specialized expertise and a thorough understanding of the ever-evolving regulatory requirements.

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Health

Why Choose Us

Our Approach

Patient-Centric Focus

At Neoclinus, patient safety and well-being are paramount. We prioritize patient-centricity throughout the research process, ensuring ethical conduct and meaningful outcomes.

Collaborative Partnerships

We believe in the power of collaboration. By forging strong partnerships with sponsors, investigators, and regulatory agencies, we drive success through shared expertise and mutual trust.

Innovation and Technology

Harnessing the latest innovations in technology and methodology, we optimize trial efficiency, streamline processes, and accelerate the pace of medical discovery.

Team work

Neoclinus complete and effortless transparency of your entire operation at your fingertips whether it is to drive customer engagement services support.

Interested in our services? Request a quote or schedule a consultation to discuss your clinical research needs with our team of experts. Make an Appointment.

Professional Medical Care In Full Measure

From protocol development to site selection and monitoring, we manage every aspect of your clinical trial to ensure timely completion and regulatory compliance.